KIP Infrastructure
2.12.0 - ci-build
KIP Infrastructure, published by Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S. This guide is not an authorized publication; it is the continuous build for version 2.12.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/KIP-infrastructure/implementation-guide/ and changes regularly. See the Directory of published versions
| Active as of 2024-01-10 |
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<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ValueSet PRDcodes</b></p><a name="PRDcodes"> </a><a name="hcPRDcodes"> </a><ul><li>Include these codes as defined in <a href="CodeSystem-PRDcodes.html"><code>https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2513">prd2513</a></td><td>2513 - AA amyloid secondary to chronic inflammation</td><td>AA amyloid secondary to chronic inflammation</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1768">prd1768</a></td><td>1768 - Acquired obstructive nephropathy due to neurogenic bladder</td><td>Acquired obstructive nephropathy due to neurogenic bladder</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1752">prd1752</a></td><td>1752 - Acquired obstructive uropathy / nephropathy </td><td>Acquired obstructive uropathy / nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3442">prd3442</a></td><td>3442 - Acute cortical necrosis</td><td>Acute cortical necrosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3380">prd3380</a></td><td>3380 - Acute kidney injury</td><td>Acute kidney injury</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3403">prd3403</a></td><td>3403 - Acute kidney injury due to circulatory failure</td><td>Acute kidney injury due to circulatory failure</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3398">prd3398</a></td><td>3398 - Acute kidney injury due to hypovolaemia </td><td>Acute kidney injury due to hypovolaemia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3435">prd3435</a></td><td>3435 - Acute kidney injury due to nephrotoxicity</td><td>Acute kidney injury due to nephrotoxicity</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3426">prd3426</a></td><td>3426 - Acute kidney injury due to rhabdomyolysis</td><td>Acute kidney injury due to rhabdomyolysis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3419">prd3419</a></td><td>3419 - Acute kidney injury due to sepsis</td><td>Acute kidney injury due to sepsis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3457">prd3457</a></td><td>3457 - Acute pyelonephritis</td><td>Acute pyelonephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2196">prd2196</a></td><td>2196 - Acute urate nephropathy - histologically proven</td><td>Acute urate nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2183">prd2183</a></td><td>2183 - Acute urate nephropathy - no histology</td><td>Acute urate nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1003">prd1003</a></td><td>1003 - Adult nephrotic syndrome - no histology</td><td>Adult nephrotic syndrome - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2392">prd2392</a></td><td>2392 - Ageing kidney - no histology</td><td>Ageing kidney - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2521">prd2521</a></td><td>2521 - AL amyloid secondary to plasma cell dyscrasia</td><td>AL amyloid secondary to plasma cell dyscrasia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3071">prd3071</a></td><td>3071 - Alagille syndrome</td><td>Alagille syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2760">prd2760</a></td><td>2760 - Alport syndrome - histologically proven</td><td>Alport syndrome - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2756">prd2756</a></td><td>2756 - Alport syndrome - no histology</td><td>Alport syndrome - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1472">prd1472</a></td><td>1472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven</td><td>Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1464">prd1464</a></td><td>1464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology</td><td>Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3118">prd3118</a></td><td>3118 - Apparent mineralocorticoid excess</td><td>Apparent mineralocorticoid excess</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1995">prd1995</a></td><td>1995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven</td><td>Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1982">prd1982</a></td><td>1982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology</td><td>Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2448">prd2448</a></td><td>2448 - Atheroembolic renal disease - histologically proven</td><td>Atheroembolic renal disease - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2430">prd2430</a></td><td>2430 - Atheroembolic renal disease - no histology</td><td>Atheroembolic renal disease - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2623">prd2623</a></td><td>2623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative</td><td>Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2718">prd2718</a></td><td>2718 - Autosomal dominant (AD) polycystic kidney disease</td><td>Autosomal dominant (AD) polycystic kidney disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2725">prd2725</a></td><td>2725 - Autosomal dominant (AD) polycystic kidney disease type I</td><td>Autosomal dominant (AD) polycystic kidney disease type I</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2739">prd2739</a></td><td>2739 - Autosomal dominant (AD) polycystic kidney disease type II</td><td>Autosomal dominant (AD) polycystic kidney disease type II</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2741">prd2741</a></td><td>2741 - Autosomal recessive (AR) polycystic kidney disease</td><td>Autosomal recessive (AR) polycystic kidney disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3085">prd3085</a></td><td>3085 - Bartter syndrome</td><td>Bartter syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2773">prd2773</a></td><td>2773 - Benign familial haematuria</td><td>Benign familial haematuria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1710">prd1710</a></td><td>1710 - Bladder exstrophy</td><td>Bladder exstrophy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3322">prd3322</a></td><td>3322 - Branchio-oto-renal syndrome</td><td>Branchio-oto-renal syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1845">prd1845</a></td><td>1845 - Calcium oxalate urolithiasis</td><td>Calcium oxalate urolithiasis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1832">prd1832</a></td><td>1832 - Calculus nephropathy / urolithiasis</td><td>Calculus nephropathy / urolithiasis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2482">prd2482</a></td><td>2482 - Cardiorenal syndrome</td><td>Cardiorenal syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2363">prd2363</a></td><td>2363 - Chronic hypertensive nephropathy - histologically proven</td><td>Chronic hypertensive nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2359">prd2359</a></td><td>2359 - Chronic hypertensive nephropathy - no histology</td><td>Chronic hypertensive nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3564">prd3564</a></td><td>3564 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven</td><td>Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3555">prd3555</a></td><td>3555 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology</td><td>Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3529">prd3529</a></td><td>3529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy</td><td>Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3540">prd3540</a></td><td>3540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy</td><td>Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3538">prd3538</a></td><td>3538 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney</td><td>Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3708">prd3708</a></td><td>3708 - Chronic renal failure</td><td>Chronic renal failure</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3643">prd3643</a></td><td>3643 - Chronic renal failure due to systemic infection</td><td>Chronic renal failure due to systemic infection</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2203">prd2203</a></td><td>2203 - Chronic urate nephropathy - histologically proven</td><td>Chronic urate nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3636">prd3636</a></td><td>3636 - Chronic urate nephropathy - no histology</td><td>Chronic urate nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1440">prd1440</a></td><td>1440 - Churg-Strauss syndrome - histologically proven</td><td>Churg-Strauss syndrome - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1438">prd1438</a></td><td>1438 - Churg-Strauss syndrome - no histology</td><td>Churg-Strauss syndrome - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1625">prd1625</a></td><td>1625 - Congenital dysplasia / hypoplasia</td><td>Congenital dysplasia / hypoplasia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2652">prd2652</a></td><td>2652 - Congenital haemolytic uraemic syndrome</td><td>Congenital haemolytic uraemic syndrome (HUS)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1088">prd1088</a></td><td>1088 - Congenital nephrotic syndrome (CNS) - congenital infection</td><td>Congenital nephrotic syndrome (CNS) - congenital infection</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1057">prd1057</a></td><td>1057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis</td><td>Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1042">prd1042</a></td><td>1042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven</td><td>Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1035">prd1035</a></td><td>1035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histology</td><td>Congenital nephrotic syndrome (CNS) - Finnish type - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1061">prd1061</a></td><td>1061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis</td><td>Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1026">prd1026</a></td><td>1026 - Congenital nephrotic syndrome - no histology</td><td>Congenital nephrotic syndrome (CNS) - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1706">prd1706</a></td><td>1706 - Congenital neurogenic bladder</td><td>Congenital neurogenic bladder</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1660">prd1660</a></td><td>1660 - Congenital pelvi-ureteric junction obstruction</td><td>Congenital pelvi-ureteric junction obstruction</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1673">prd1673</a></td><td>1673 - Congenital vesico-ureteric junction obstruction</td><td>Congenital vesico-ureteric junction obstruction</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1570">prd1570</a></td><td>1570 - Cryoglobulinaemia secondary to hepatitis C - histologically proven</td><td>Cryoglobulinaemia secondary to hepatitis C - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1562">prd1562</a></td><td>1562 - Cryoglobulinaemia secondary to hepatitis C - no histology</td><td>Cryoglobulinaemia secondary to hepatitis C - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1591">prd1591</a></td><td>1591 - Cryoglobulinaemia secondary to systemic disease - histologically proven</td><td>Cryoglobulinaemia secondary to systemic disease - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1589">prd1589</a></td><td>1589 - Cryoglobulinaemia secondary to systemic disease - no histology</td><td>Cryoglobulinaemia secondary to systemic disease - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2794">prd2794</a></td><td>2794 - Cystic kidney disease</td><td>Cystic kidney disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2964">prd2964</a></td><td>2964 - Cystinosis</td><td>Cystinosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2955">prd2955</a></td><td>2955 - Cystinuria</td><td>Cystinuria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2929">prd2929</a></td><td>2929 - Dent disease</td><td>Dent disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1074">prd1074</a></td><td>1074 - Denys-Drash syndrome</td><td>Denys-Drash syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2328">prd2328</a></td><td>2328 - Diabetic nephropathy in type I diabetes - histologically proven</td><td>Diabetic nephropathy in type I diabetes - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2316">prd2316</a></td><td>2316 - Diabetic nephropathy in type I diabetes - no histology</td><td>Diabetic nephropathy in type I diabetes - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2344">prd2344</a></td><td>2344 - Diabetic nephropathy in type II diabetes - histologically proven</td><td>Diabetic nephropathy in type II diabetes - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2337">prd2337</a></td><td>2337 - Diabetic nephropathy in type II diabetes - no histology</td><td>Diabetic nephropathy in type II diabetes - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1331">prd1331</a></td><td>1331 - Diffuse endocapillary glomerulonephritis</td><td>Diffuse endocapillary glomerulonephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3028">prd3028</a></td><td>3028 - Distal renal tubular acidosis - type I</td><td>Distal renal tubular acidosis (RTA) - type I</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3037">prd3037</a></td><td>3037 - Distal renal tubular acidosis with sensorineural deafness - gene mutations</td><td>Distal renal tubular acidosis with sensorineural deafness - gene mutations</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2005">prd2005</a></td><td>2005 - Drug-induced tubulointerstitial nephritis - no histology</td><td>Drug-induced tubulointerstitial nephritis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2014">prd2014</a></td><td>2014 - Drug-induced tubulointerstitial nephritis - histologically proven</td><td>Drug-induced tubulointerstitial nephritis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1850">prd1850</a></td><td>1850 - Enteric hyperoxaluria</td><td>Enteric hyperoxaluria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1558">prd1558</a></td><td>1558 - Essential mixed cryoglobulinaemia - histologically proven</td><td>Essential mixed cryoglobulinaemia - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1543">prd1543</a></td><td>1543 - Essential mixed cryoglobulinaemia - no histology</td><td>Essential mixed cryoglobulinaemia - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3230">prd3230</a></td><td>3230 - Fabry disease - histologically proven</td><td>Fabry disease - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3224">prd3224</a></td><td>3224 - Fabry disease - no histology</td><td>Fabry disease - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2545">prd2545</a></td><td>2545 - Familial amyloid secondary to protein mutations - histologically proven</td><td>Familial amyloid secondary to protein mutations - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2532">prd2532</a></td><td>2532 - Familial amyloid secondary to protein mutations - no histology</td><td>Familial amyloid secondary to protein mutations - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1308">prd1308</a></td><td>1308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven</td><td>Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1298">prd1298</a></td><td>1298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology</td><td>Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1280">prd1280</a></td><td>1280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven</td><td>Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1279">prd1279</a></td><td>1279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology</td><td>Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2668">prd2668</a></td><td>2668 - Familial haemolytic uraemic syndrome (HUS)</td><td>Familial haemolytic uraemic syndrome (HUS)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3173">prd3173</a></td><td>3173 - Familial hypercalciuric hypocalcaemia</td><td>Familial hypercalciuric hypocalcaemia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3160">prd3160</a></td><td>3160 - Familial hypocalciuric hypercalcaemia</td><td>Familial hypocalciuric hypercalcaemia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3187">prd3187</a></td><td>3187 - Familial hypomagnesaemia</td><td>Familial hypomagnesaemia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1144">prd1144</a></td><td>1144 - Familial IgA nephropathy - histologically proven</td><td>Familial IgA nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1137">prd1137</a></td><td>1137 - Familial IgA nephropathy - no histology</td><td>Familial IgA nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1911">prd1911</a></td><td>1911 - Familial interstitial nephropathy - histologically proven</td><td>Familial interstitial nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1907">prd1907</a></td><td>1907 - Familial interstitial nephropathy - no histology</td><td>Familial interstitial nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3379">prd3379</a></td><td>3379 - Familial nephropathy</td><td>Familial nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1618">prd1618</a></td><td>1618 - Familial reflux nephropathy</td><td>Familial reflux nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2675">prd2675</a></td><td>2675 - Familial thrombotic thrombocytopenic purpura(2675)</td><td>Familial thrombotic thrombocytopenic purpura (TTP)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2566">prd2566</a></td><td>2566 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven</td><td>Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2550">prd2550</a></td><td>2550 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology</td><td>Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2453">prd2453</a></td><td>2453 - Fibromuscular dysplasia of renal artery</td><td>Fibromuscular dysplasia of renal artery</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1354">prd1354</a></td><td>1354 - Focal and segmental proliferative glomerulonephritis</td><td>Focal and segmental proliferative glomerulonephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3754">prd3754</a></td><td>3754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV </td><td>Focal segmental glomerulosclerosis (FSGS) secondary to HIV</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3765">prd3765</a></td><td>3765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium </td><td>Focal segmental glomerulosclerosis (FSGS) secondary to lithium</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1320">prd1320</a></td><td>1320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven</td><td>Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1312">prd1312</a></td><td>1312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology</td><td>Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3777">prd3777</a></td><td>3777 - Focal segmental glomerulosclerosis secondary to sickle cell</td><td>Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3314">prd3314</a></td><td>3314 - Frasier syndrome</td><td>Frasier syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3092">prd3092</a></td><td>3092 - Gitelman syndrome</td><td>Gitelman syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1656">prd1656</a></td><td>1656 - Glomerulocystic disease</td><td>Glomerulocystic disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1377">prd1377</a></td><td>1377 - Glomerulonephritis - histologically indeterminate</td><td>Glomerulonephritis - histologically indeterminate</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3749">prd3749</a></td><td>3749 - Glomerulonephritis - no histology</td><td>Glomerulonephritis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1365">prd1365</a></td><td>1365 - Glomerulonephritis - secondary to systemic disease</td><td>Glomerulonephritis - secondary to systemic disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3125">prd3125</a></td><td>3125 - Glucocorticoid suppressible hyperaldosteronism</td><td>Glucocorticoid suppressible hyperaldosteronism</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1417">prd1417</a></td><td>1417 - Granulomatosis with polyangiitis - histologically proven</td><td>Granulomatosis with polyangiitis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1401">prd1401</a></td><td>1401 - Granulomatosis with polyangiitis - no histology</td><td>Granulomatosis with polyangiitis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3572">prd3572</a></td><td>3572 - Haematuria and proteinuria - no histology</td><td>Haematuria and proteinuria - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2610">prd2610</a></td><td>2610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associated</td><td>Haemolytic uraemic syndrome (HUS) - diarrhoea associated</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2647">prd2647</a></td><td>2647 - Haemolytic uraemic syndrome (HUS) secondary to systemic disease</td><td>Haemolytic uraemic syndrome (HUS) secondary to systemic disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2257">prd2257</a></td><td>2257 - Hantavirus nephropathy</td><td>Hantavirus nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1515">prd1515</a></td><td>1515 - Henoch-Schönlein purpura / nephritis - histologically proven</td><td>Henoch-Schönlein purpura / nephritis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1504">prd1504</a></td><td>1504 - Henoch-Schönlein purpura / nephritis - no histology</td><td>Henoch-Schönlein purpura / nephritis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2495">prd2495</a></td><td>2495 - Hepatorenal syndrome</td><td>Hepatorenal syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3305">prd3305</a></td><td>3305 - Horse-shoe kidney</td><td>Horse-shoe kidney</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3662">prd3662</a></td><td>3662 - Hypercalcaemic nephropathy</td><td>Hypercalcaemic nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2993">prd2993</a></td><td>2993 - Hypophosphataemic rickets autosomal recessive (AR)</td><td>Hypophosphataemic rickets autosomal recessive (AR)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2986">prd2986</a></td><td>2986 - Hypophosphataemic rickets X-linked (XL)</td><td>Hypophosphataemic rickets X-linked (XL)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1251">prd1251</a></td><td>1251 - Idiopathic rapidly progressive (crescentic) glomerulonephritis</td><td>Idiopathic rapidly progressive (crescentic) glomerulonephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1813">prd1813</a></td><td>1813 - Idiopathic retroperitoneal fibrosis</td><td>Idiopathic retroperitoneal fibrosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1128">prd1128</a></td><td>1128 - IgA nephropathy - histologically proven</td><td>IgA nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1116">prd1116</a></td><td>1116 - IgA nephropathy - no histology</td><td>IgA nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1163">prd1163</a></td><td>1163 - IgA nephropathy secondary to liver cirrhosis - histologically proven</td><td>IgA nephropathy secondary to liver cirrhosis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1159">prd1159</a></td><td>1159 - IgA nephropathy secondary to liver cirrhosis - no histology</td><td>IgA nephropathy secondary to liver cirrhosis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1171">prd1171</a></td><td>1171 - IgM - associated nephropathy</td><td>IgM - associated nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2606">prd2606</a></td><td>2606 - Immunotactoid / fibrillary nephropathy</td><td>Immunotactoid / fibrillary nephropathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3823">prd3823</a></td><td>3823 - Infiltration by lymphoma - histologically proven</td><td>Infiltration by lymphoma - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3139">prd3139</a></td><td>3139 - Inherited / genetic diabetes mellitus type II</td><td>Inherited / genetic diabetes mellitus type II</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2940">prd2940</a></td><td>2940 - Inherited aminoaciduria</td><td>Inherited aminoaciduria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2972">prd2972</a></td><td>2972 - Inherited renal glycosuria</td><td>Inherited renal glycosuria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2407">prd2407</a></td><td>2407 - Ischaemic nephropathy - no histology</td><td>Ischaemic nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2411">prd2411</a></td><td>2411 - Ischaemic nephropathy / microvascular disease - histologically proven</td><td>Ischaemic nephropathy / microvascular disease - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3712">prd3712</a></td><td>3712 - Isolated haematuria - no histology</td><td>Isolated haematuria - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3720">prd3720</a></td><td>3720 - Isolated proteinuria - no histology</td><td>Isolated proteinuria - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3810">prd3810</a></td><td>3810 - Kidney stones due to ARPT deficiency</td><td>Kidney stones due to ARPT deficiency</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3461">prd3461</a></td><td>3461 - Kidney tumour</td><td>Kidney tumour</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3351">prd3351</a></td><td>3351 - Lawrence-Moon-Biedl / Bardet-Biedl syndrome</td><td>Lawrence-Moon-Biedl / Bardet-Biedl syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2177">prd2177</a></td><td>2177 - Lead induced nephropathy - histologically proven</td><td>Lead induced nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2165">prd2165</a></td><td>2165 - Lead induced nephropathy - no histology</td><td>Lead induced nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2242">prd2242</a></td><td>2242 - Leptospirosis</td><td>Leptospirosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3059">prd3059</a></td><td>3059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency</td><td>Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3102">prd3102</a></td><td>3102 - Liddle syndrome</td><td>Liddle syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2597">prd2597</a></td><td>2597 - Light chain deposition disease</td><td>Light chain deposition disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2938">prd2938</a></td><td>2938 - Lowe syndrome (oculocerebrorenal syndrome)</td><td>Lowe syndrome (oculocerebrorenal syndrome)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1866">prd1866</a></td><td>1866 - Magnesium ammonium phosphate (struvite) urolithiasis</td><td>Magnesium ammonium phosphate (struvite) urolithiasis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2385">prd2385</a></td><td>2385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven</td><td>Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2371">prd2371</a></td><td>2371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology</td><td>Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2804">prd2804</a></td><td>2804 - Medullary cystic kidney disease type I</td><td>Medullary cystic kidney disease type I</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2815">prd2815</a></td><td>2815 - Medullary cystic kidney disease type II</td><td>Medullary cystic kidney disease type II</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3295">prd3295</a></td><td>3295 - Medullary sponge kidneys</td><td>Medullary sponge kidneys</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1723">prd1723</a></td><td>1723 - Megacystis-megaureter</td><td>Megacystis-megaureter</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1205">prd1205</a></td><td>1205 - Membranous nephropathy - drug induced</td><td>Membranous nephropathy - drug induced</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1185">prd1185</a></td><td>1185 - Membranous nephropathy - idiopathic</td><td>Membranous nephropathy - idiopathic</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1214">prd1214</a></td><td>1214 - Membranous nephropathy - infection associated</td><td>Membranous nephropathy - infection associated</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1192">prd1192</a></td><td>1192 - Membranous nephropathy - malignancy associated</td><td>Membranous nephropathy - malignancy associated</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1349">prd1349</a></td><td>1349 - Mesangial proliferative glomerulonephritis </td><td>Mesangial proliferative glomerulonephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1222">prd1222</a></td><td>1222 - Mesangiocapillary glomerulonephritis type 1</td><td>Mesangiocapillary glomerulonephritis type 1</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1233">prd1233</a></td><td>1233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)</td><td>Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1246">prd1246</a></td><td>1246 - Mesangiocapillary glomerulonephritis type 3</td><td>Mesangiocapillary glomerulonephritis type 3</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3501">prd3501</a></td><td>3501 - Mesoblastic nephroma - histologically proven</td><td>Mesoblastic nephroma - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1429">prd1429</a></td><td>1429 - Microscopic polyangiitis - histologically proven</td><td>Microscopic polyangiitis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1100">prd1100</a></td><td>1100 - Minimal change nephropathy - histologically proven</td><td>Minimal change nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1090">prd1090</a></td><td>1090 - Minimal change nephropathy - no histology</td><td>Minimal change nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3367">prd3367</a></td><td>3367 - Mitochondrial cytopathy</td><td>Mitochondrial cytopathy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1639">prd1639</a></td><td>1639 - Multicystic dysplastic kidneys</td><td>Multicystic dysplastic kidneys</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2584">prd2584</a></td><td>2584 - Myeloma cast nephropathy - histologically proven</td><td>Myeloma cast nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2578">prd2578</a></td><td>2578 - Myeloma kidney - no histology</td><td>Myeloma kidney - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3253">prd3253</a></td><td>3253 - Nail-patella syndrome</td><td>Nail-patella syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3044">prd3044</a></td><td>3044 - Nephrogenic diabetes insipidus</td><td>Nephrogenic diabetes insipidus</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2836">prd2836</a></td><td>2836 - Nephronophthisis</td><td>Nephronophthisis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2843">prd2843</a></td><td>2843 - Nephronophthisis - type 1 (juvenile type)</td><td>Nephronophthisis - type 1 (juvenile type)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2858">prd2858</a></td><td>2858 - Nephronophthisis - type 2 (infantile type)</td><td>Nephronophthisis - type 2 (infantile type)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2862">prd2862</a></td><td>2862 - Nephronophthisis - type 3 (adolescent type)</td><td>Nephronophthisis - type 3 (adolescent type)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2870">prd2870</a></td><td>2870 - Nephronophthisis - type 4 (juvenile type)</td><td>Nephronophthisis - type 4 (juvenile type)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2889">prd2889</a></td><td>2889 - Nephronophthisis - type 5</td><td>Nephronophthisis - type 5</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2891">prd2891</a></td><td>2891 - Nephronophthisis - type 6</td><td>Nephronophthisis - type 6</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2098">prd2098</a></td><td>2098 - Nephropathy due to aminoglycosides - histologically proven</td><td>Nephropathy due to aminoglycosides - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2080">prd2080</a></td><td>2080 - Nephropathy due to aminoglycosides - no histology</td><td>Nephropathy due to aminoglycosides - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2112">prd2112</a></td><td>2112 - Nephropathy due to amphotericin - histologically proven</td><td>Nephropathy due to amphotericin - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2108">prd2108</a></td><td>2108 - Nephropathy due to amphotericin - no histology</td><td>Nephropathy due to amphotericin - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2033">prd2033</a></td><td>2033 - Nephropathy due to analgesic drugs - histologically proven</td><td>Nephropathy due to analgesic drugs - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2022">prd2022</a></td><td>2022 - Nephropathy due to analgesic drugs - no histology</td><td>Nephropathy due to analgesic drugs - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2051">prd2051</a></td><td>2051 - Nephropathy due to ciclosporin - histologically proven</td><td>Nephropathy due to ciclosporin - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2046">prd2046</a></td><td>2046 - Nephropathy due to ciclosporin - no histology</td><td>Nephropathy due to ciclosporin - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2131">prd2131</a></td><td>2131 - Nephropathy due to cisplatin - histologically proven</td><td>Nephropathy due to cisplatin - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2120">prd2120</a></td><td>2120 - Nephropathy due to cisplatin - no histology</td><td>Nephropathy due to cisplatin - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2681">prd2681</a></td><td>2681 - Nephropathy due to eclampsia</td><td>Nephropathy due to eclampsia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2154">prd2154</a></td><td>2154 - Nephropathy due to lithium - histologically proven</td><td>Nephropathy due to lithium - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2149">prd2149</a></td><td>2149 - Nephropathy due to lithium - no histology</td><td>Nephropathy due to lithium - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3834">prd3834</a></td><td>3834 - Nephropathy due to pre-eclampsia</td><td>Nephropathy due to pre-eclampsia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2079">prd2079</a></td><td>2079 - Nephropathy due to tacrolimus - histologically proven</td><td>Nephropathy due to tacrolimus - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2067">prd2067</a></td><td>2067 - Nephropathy due to tacrolimus - no histology</td><td>Nephropathy due to tacrolimus - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2288">prd2288</a></td><td>2288 - Nephropathy related to HIV - histologically proven</td><td>Nephropathy related to HIV - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2274">prd2274</a></td><td>2274 - Nephropathy related to HIV - no histology</td><td>Nephropathy related to HIV - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3615">prd3615</a></td><td>3615 - Nephrotic syndrome of childhood - no trial of steroids - no histology</td><td>Nephrotic syndrome of childhood - no trial of steroids - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3604">prd3604</a></td><td>3604 - Nephrotic syndrome of childhood - steroid resistant - no histology</td><td>Nephrotic syndrome of childhood - steroid resistant - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1019">prd1019</a></td><td>1019 - Nephrotic syndrome of childhood - steroid sensitive - no histology</td><td>Nephrotic syndrome of childhood - steroid sensitive - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1799">prd1799</a></td><td>1799 - Obstructive nephropathy due to bladder cancer</td><td>Obstructive nephropathy due to bladder cancer</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1809">prd1809</a></td><td>1809 - Obstructive nephropathy due to other malignancies</td><td>Obstructive nephropathy due to other malignancies</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1781">prd1781</a></td><td>1781 - Obstructive nephropathy due to prostate cancer</td><td>Obstructive nephropathy due to prostate cancer</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1775">prd1775</a></td><td>1775 - Obstructive nephropathy due to prostatic hypertrophy</td><td>Obstructive nephropathy due to prostatic hypertrophy</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1734">prd1734</a></td><td>1734 - Oligomeganephronia</td><td>Oligomeganephronia</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2300">prd2300</a></td><td>2300 - Other specific infection</td><td>Other specific infection</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3063">prd3063</a></td><td>3063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity</td><td>Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1455">prd1455</a></td><td>1455 - Polyarteritis nodosa</td><td>Polyarteritis nodosa</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1687">prd1687</a></td><td>1687 - Posterior urethral valves</td><td>Posterior urethral valves</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2901">prd2901</a></td><td>2901 - Primary Fanconi syndrome</td><td>Primary Fanconi syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1267">prd1267</a></td><td>1267 - Primary focal segmental glomerulosclerosis (FSGS)</td><td>Primary focal segmental glomerulosclerosis (FSGS)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3194">prd3194</a></td><td>3194 - Primary hyperoxaluria</td><td>Primary hyperoxaluria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3207">prd3207</a></td><td>3207 - Primary hyperoxaluria type I</td><td>Primary hyperoxaluria type I</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3211">prd3211</a></td><td>3211 - Primary hyperoxaluria type II</td><td>Primary hyperoxaluria type II</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3731">prd3731</a></td><td>3731 - Primary hyperoxaluria type III</td><td>Primary hyperoxaluria type III</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1602">prd1602</a></td><td>1602 - Primary reflux nephropathy - sporadic</td><td>Primary reflux nephropathy - sporadic</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3000">prd3000</a></td><td>3000 - Primary renal tubular acidosis (RTA)</td><td>Primary renal tubular acidosis (RTA)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3016">prd3016</a></td><td>3016 - Proximal renal tubular acidosis (RTA) - type II</td><td>Proximal renal tubular acidosis (RTA) - type II</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3141">prd3141</a></td><td>3141 - Pseudohypoaldosteronism type 1</td><td>Pseudohypoaldosteronism type 1</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3156">prd3156</a></td><td>3156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)</td><td>Pseudohypoaldosteronism type 2 (Gordon syndrome)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2219">prd2219</a></td><td>2219 - Radiation nephritis</td><td>Radiation nephritis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2226">prd2226</a></td><td>2226 - Renal / perinephric abscess</td><td>Renal / perinephric abscess</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2509">prd2509</a></td><td>2509 - Renal amyloidosis</td><td>Renal amyloidosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2469">prd2469</a></td><td>2469 - Renal arterial thrombosis / occlusion</td><td>Renal arterial thrombosis / occlusion</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2424">prd2424</a></td><td>2424 - Renal artery stenosis</td><td>Renal artery stenosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3474">prd3474</a></td><td>3474 - Renal cell carcinoma - histologically proven</td><td>Renal cell carcinoma - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3658">prd3658</a></td><td>3658 - Renal coloboma syndrome</td><td>Renal coloboma syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3627">prd3627</a></td><td>3627 - Renal cysts and diabetes syndrome</td><td>Renal cysts and diabetes syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1641">prd1641</a></td><td>1641 - Renal dysplasia due to fetal ACE-inhibitor exposure</td><td>Renal dysplasia due to fetal ACE-inhibitor exposure</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3691">prd3691</a></td><td>3691 - Renal failure</td><td>Renal failure</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1747">prd1747</a></td><td>1747 - Renal papillary necrosis</td><td>Renal papillary necrosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3796">prd3796</a></td><td>3796 - Renal papillary necrosis caused by analgesics</td><td>Renal papillary necrosis caused by analgesics</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3783">prd3783</a></td><td>3783 - Renal papillary necrosis caused by diabetes</td><td>Renal papillary necrosis caused by diabetes</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3806">prd3806</a></td><td>3806 - Renal papillary necrosis caused by sickle cell</td><td>Renal papillary necrosis caused by sickle cell</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1976">prd1976</a></td><td>1976 - Renal sarcoidosis - histologically proven</td><td>Renal sarcoidosis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1969">prd1969</a></td><td>1969 - Renal sarcoidosis - no histology</td><td>Renal sarcoidosis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1536">prd1536</a></td><td>1536 - Renal scleroderma / systemic sclerosis - histologically proven</td><td>Renal scleroderma / systemic sclerosis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1527">prd1527</a></td><td>1527 - Renal scleroderma / systemic sclerosis - no histology</td><td>Renal scleroderma / systemic sclerosis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2235">prd2235</a></td><td>2235 - Renal tuberculosis</td><td>Renal tuberculosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2476">prd2476</a></td><td>2476 - Renal vein thrombosis</td><td>Renal vein thrombosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3689">prd3689</a></td><td>3689 - Retroperitoneal fibrosis secondary to drugs</td><td>Retroperitoneal fibrosis secondary to drugs</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1821">prd1821</a></td><td>1821 - Retroperitoneal fibrosis secondary to malignancies</td><td>Retroperitoneal fibrosis secondary to malignancies</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3670">prd3670</a></td><td>3670 - Retroperitoneal fibrosis secondary to peri-aortitis</td><td>Retroperitoneal fibrosis secondary to peri-aortitis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3269">prd3269</a></td><td>3269 - Rubinstein-Taybi syndrome</td><td>Rubinstein-Taybi syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2290">prd2290</a></td><td>2290 - Schistosomiasis</td><td>Schistosomiasis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2702">prd2702</a></td><td>2702 - Sickle cell nephropathy - histologically proven</td><td>Sickle cell nephropathy - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2699">prd2699</a></td><td>2699 - Sickle cell nephropathy - no histology</td><td>Sickle cell nephropathy - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3517">prd3517</a></td><td>3517 - Single kidney identified in adulthood</td><td>Single kidney identified in adulthood</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1694">prd1694</a></td><td>1694 - Syndrome of agenesis of abdominal muscles - prune belly syndrome</td><td>Syndrome of agenesis of abdominal muscles - prune belly syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1493">prd1493</a></td><td>1493 - Systemic lupus erythematosus / nephritis - histologically proven</td><td>Systemic lupus erythematosus / nephritis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1486">prd1486</a></td><td>1486 - Systemic lupus erythematosus / nephritis - no histology</td><td>Systemic lupus erythematosus / nephritis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1383">prd1383</a></td><td>1383 - Systemic vasculitis - ANCA negative - histologically proven</td><td>Systemic vasculitis - ANCA negative - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3847">prd3847</a></td><td>3847 - Systemic vasculitis - ANCA negative - no histology</td><td>Systemic vasculitis - ANCA negative - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3852">prd3852</a></td><td>3852 - Systemic vasculitis - ANCA positive - histologically proven</td><td>Systemic vasculitis - ANCA positive - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1396">prd1396</a></td><td>1396 - Systemic vasculitis - ANCA positive - no histology</td><td>Systemic vasculitis - ANCA positive - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2787">prd2787</a></td><td>2787 - Thin basement membrane disease</td><td>Thin basement membrane disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2634">prd2634</a></td><td>2634 - Thrombotic thrombocytopenic purpura (TTP)</td><td>Thrombotic thrombocytopenic purpura (TTP)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3346">prd3346</a></td><td>3346 - Townes-Brocks syndrome</td><td>Townes-Brocks syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3488">prd3488</a></td><td>3488 - Transitional cell carcinoma - histologically proven</td><td>Transitional cell carcinoma - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3276">prd3276</a></td><td>3276 - Tuberous sclerosis</td><td>Tuberous sclerosis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2917">prd2917</a></td><td>2917 - Tubular disorder as part of inherited metabolic diseases</td><td>Tubular disorder as part of inherited metabolic diseases</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1897">prd1897</a></td><td>1897 - Tubulointerstitial nephritis - histologically proven</td><td>Tubulointerstitial nephritis - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1884">prd1884</a></td><td>1884 - Tubulointerstitial nephritis - no histology</td><td>Tubulointerstitial nephritis - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1930">prd1930</a></td><td>1930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically proven</td><td>Tubulointerstitial nephritis associated with autoimmune disease - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1924">prd1924</a></td><td>1924 - Tubulointerstitial nephritis associated with autoimmune disease - no histology</td><td>Tubulointerstitial nephritis associated with autoimmune disease - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1953">prd1953</a></td><td>1953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically proven</td><td>Tubulointerstitial nephritis with uveitis (TINU) - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1948">prd1948</a></td><td>1948 - Tubulointerstitial nephritis with uveitis (TINU) - no histology</td><td>Tubulointerstitial nephritis with uveitis (TINU) - no histology</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd1878">prd1878</a></td><td>1878 - Uric acid urolithiasis</td><td>Uric acid urolithiasis</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2827">prd2827</a></td><td>2827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)</td><td>Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3282">prd3282</a></td><td>3282 - Von Hippel-Lindau disease</td><td>Von Hippel-Lindau disease</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3333">prd3333</a></td><td>3333 - Williams syndrome</td><td>Williams syndrome</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3490">prd3490</a></td><td>3490 - Wilms tumour - histologically proven</td><td>Wilms tumour - histologically proven</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd3248">prd3248</a></td><td>3248 - Xanthinuria</td><td>Xanthinuria</td></tr><tr><td><a href="CodeSystem-PRDcodes.html#PRDcodes-prd2261">prd2261</a></td><td>2261 - Xanthogranulomatous pyelonephritis</td><td>Xanthogranulomatous pyelonephritis</td></tr></table></li></ul></div>
</text>
<url value="https://kip.rkkp.dk/fhir/ValueSet/PRDcodes"/>
<version value="2.12.0"/>
<name value="PRDcodes"/>
<title value="ERA PRD Codes"/>
<status value="active"/>
<experimental value="true"/>
<date value="2024-01-10T00:00:00+02:00"/>
<publisher
value="Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S"/>
<contact>
<name
value="Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S"/>
<telecom>
<system value="url"/>
<value value="https://trifork.com"/>
</telecom>
<telecom>
<system value="email"/>
<value value="rbk@trifork.com"/>
</telecom>
</contact>
<description
value="European Renal Association (ERA) Primary Renal Disease (PRD)"/>
<compose>
<include>
<system value="https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes"/>
<concept>
<code value="prd2513"/>
<display value="2513 - AA amyloid secondary to chronic inflammation"/>
</concept>
<concept>
<code value="prd1768"/>
<display
value="1768 - Acquired obstructive nephropathy due to neurogenic bladder"/>
</concept>
<concept>
<code value="prd1752"/>
<display value="1752 - Acquired obstructive uropathy / nephropathy "/>
</concept>
<concept>
<code value="prd3442"/>
<display value="3442 - Acute cortical necrosis"/>
</concept>
<concept>
<code value="prd3380"/>
<display value="3380 - Acute kidney injury"/>
</concept>
<concept>
<code value="prd3403"/>
<display
value="3403 - Acute kidney injury due to circulatory failure"/>
</concept>
<concept>
<code value="prd3398"/>
<display value="3398 - Acute kidney injury due to hypovolaemia "/>
</concept>
<concept>
<code value="prd3435"/>
<display value="3435 - Acute kidney injury due to nephrotoxicity"/>
</concept>
<concept>
<code value="prd3426"/>
<display value="3426 - Acute kidney injury due to rhabdomyolysis"/>
</concept>
<concept>
<code value="prd3419"/>
<display value="3419 - Acute kidney injury due to sepsis"/>
</concept>
<concept>
<code value="prd3457"/>
<display value="3457 - Acute pyelonephritis"/>
</concept>
<concept>
<code value="prd2196"/>
<display
value="2196 - Acute urate nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2183"/>
<display value="2183 - Acute urate nephropathy - no histology"/>
</concept>
<concept>
<code value="prd1003"/>
<display value="1003 - Adult nephrotic syndrome - no histology"/>
</concept>
<concept>
<code value="prd2392"/>
<display value="2392 - Ageing kidney - no histology"/>
</concept>
<concept>
<code value="prd2521"/>
<display
value="2521 - AL amyloid secondary to plasma cell dyscrasia"/>
</concept>
<concept>
<code value="prd3071"/>
<display value="3071 - Alagille syndrome"/>
</concept>
<concept>
<code value="prd2760"/>
<display value="2760 - Alport syndrome - histologically proven"/>
</concept>
<concept>
<code value="prd2756"/>
<display value="2756 - Alport syndrome - no histology"/>
</concept>
<concept>
<code value="prd1472"/>
<display
value="1472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven"/>
</concept>
<concept>
<code value="prd1464"/>
<display
value="1464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology"/>
</concept>
<concept>
<code value="prd3118"/>
<display value="3118 - Apparent mineralocorticoid excess"/>
</concept>
<concept>
<code value="prd1995"/>
<display
value="1995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven"/>
</concept>
<concept>
<code value="prd1982"/>
<display
value="1982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology"/>
</concept>
<concept>
<code value="prd2448"/>
<display
value="2448 - Atheroembolic renal disease - histologically proven"/>
</concept>
<concept>
<code value="prd2430"/>
<display value="2430 - Atheroembolic renal disease - no histology"/>
</concept>
<concept>
<code value="prd2623"/>
<display
value="2623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative"/>
</concept>
<concept>
<code value="prd2718"/>
<display
value="2718 - Autosomal dominant (AD) polycystic kidney disease"/>
</concept>
<concept>
<code value="prd2725"/>
<display
value="2725 - Autosomal dominant (AD) polycystic kidney disease type I"/>
</concept>
<concept>
<code value="prd2739"/>
<display
value="2739 - Autosomal dominant (AD) polycystic kidney disease type II"/>
</concept>
<concept>
<code value="prd2741"/>
<display
value="2741 - Autosomal recessive (AR) polycystic kidney disease"/>
</concept>
<concept>
<code value="prd3085"/>
<display value="3085 - Bartter syndrome"/>
</concept>
<concept>
<code value="prd2773"/>
<display value="2773 - Benign familial haematuria"/>
</concept>
<concept>
<code value="prd1710"/>
<display value="1710 - Bladder exstrophy"/>
</concept>
<concept>
<code value="prd3322"/>
<display value="3322 - Branchio-oto-renal syndrome"/>
</concept>
<concept>
<code value="prd1845"/>
<display value="1845 - Calcium oxalate urolithiasis"/>
</concept>
<concept>
<code value="prd1832"/>
<display value="1832 - Calculus nephropathy / urolithiasis"/>
</concept>
<concept>
<code value="prd2482"/>
<display value="2482 - Cardiorenal syndrome"/>
</concept>
<concept>
<code value="prd2363"/>
<display
value="2363 - Chronic hypertensive nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2359"/>
<display
value="2359 - Chronic hypertensive nephropathy - no histology"/>
</concept>
<concept>
<code value="prd3564"/>
<display
value="3564 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven"/>
</concept>
<concept>
<code value="prd3555"/>
<display
value="3555 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology"/>
</concept>
<concept>
<code value="prd3529"/>
<display
value="3529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy"/>
</concept>
<concept>
<code value="prd3540"/>
<display
value="3540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy"/>
</concept>
<concept>
<code value="prd3538"/>
<display
value="3538 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney"/>
</concept>
<concept>
<code value="prd3708"/>
<display value="3708 - Chronic renal failure"/>
</concept>
<concept>
<code value="prd3643"/>
<display
value="3643 - Chronic renal failure due to systemic infection"/>
</concept>
<concept>
<code value="prd2203"/>
<display
value="2203 - Chronic urate nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd3636"/>
<display value="3636 - Chronic urate nephropathy - no histology"/>
</concept>
<concept>
<code value="prd1440"/>
<display
value="1440 - Churg-Strauss syndrome - histologically proven"/>
</concept>
<concept>
<code value="prd1438"/>
<display value="1438 - Churg-Strauss syndrome - no histology"/>
</concept>
<concept>
<code value="prd1625"/>
<display value="1625 - Congenital dysplasia / hypoplasia"/>
</concept>
<concept>
<code value="prd2652"/>
<display value="2652 - Congenital haemolytic uraemic syndrome"/>
</concept>
<concept>
<code value="prd1088"/>
<display
value="1088 - Congenital nephrotic syndrome (CNS) - congenital infection"/>
</concept>
<concept>
<code value="prd1057"/>
<display
value="1057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis"/>
</concept>
<concept>
<code value="prd1042"/>
<display
value="1042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven"/>
</concept>
<concept>
<code value="prd1035"/>
<display
value="1035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histology"/>
</concept>
<concept>
<code value="prd1061"/>
<display
value="1061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis"/>
</concept>
<concept>
<code value="prd1026"/>
<display value="1026 - Congenital nephrotic syndrome - no histology"/>
</concept>
<concept>
<code value="prd1706"/>
<display value="1706 - Congenital neurogenic bladder"/>
</concept>
<concept>
<code value="prd1660"/>
<display
value="1660 - Congenital pelvi-ureteric junction obstruction"/>
</concept>
<concept>
<code value="prd1673"/>
<display
value="1673 - Congenital vesico-ureteric junction obstruction"/>
</concept>
<concept>
<code value="prd1570"/>
<display
value="1570 - Cryoglobulinaemia secondary to hepatitis C - histologically proven"/>
</concept>
<concept>
<code value="prd1562"/>
<display
value="1562 - Cryoglobulinaemia secondary to hepatitis C - no histology"/>
</concept>
<concept>
<code value="prd1591"/>
<display
value="1591 - Cryoglobulinaemia secondary to systemic disease - histologically proven"/>
</concept>
<concept>
<code value="prd1589"/>
<display
value="1589 - Cryoglobulinaemia secondary to systemic disease - no histology"/>
</concept>
<concept>
<code value="prd2794"/>
<display value="2794 - Cystic kidney disease"/>
</concept>
<concept>
<code value="prd2964"/>
<display value="2964 - Cystinosis"/>
</concept>
<concept>
<code value="prd2955"/>
<display value="2955 - Cystinuria"/>
</concept>
<concept>
<code value="prd2929"/>
<display value="2929 - Dent disease"/>
</concept>
<concept>
<code value="prd1074"/>
<display value="1074 - Denys-Drash syndrome"/>
</concept>
<concept>
<code value="prd2328"/>
<display
value="2328 - Diabetic nephropathy in type I diabetes - histologically proven"/>
</concept>
<concept>
<code value="prd2316"/>
<display
value="2316 - Diabetic nephropathy in type I diabetes - no histology"/>
</concept>
<concept>
<code value="prd2344"/>
<display
value="2344 - Diabetic nephropathy in type II diabetes - histologically proven"/>
</concept>
<concept>
<code value="prd2337"/>
<display
value="2337 - Diabetic nephropathy in type II diabetes - no histology"/>
</concept>
<concept>
<code value="prd1331"/>
<display value="1331 - Diffuse endocapillary glomerulonephritis"/>
</concept>
<concept>
<code value="prd3028"/>
<display value="3028 - Distal renal tubular acidosis - type I"/>
</concept>
<concept>
<code value="prd3037"/>
<display
value="3037 - Distal renal tubular acidosis with sensorineural deafness - gene mutations"/>
</concept>
<concept>
<code value="prd2005"/>
<display
value="2005 - Drug-induced tubulointerstitial nephritis - no histology"/>
</concept>
<concept>
<code value="prd2014"/>
<display
value="2014 - Drug-induced tubulointerstitial nephritis - histologically proven"/>
</concept>
<concept>
<code value="prd1850"/>
<display value="1850 - Enteric hyperoxaluria"/>
</concept>
<concept>
<code value="prd1558"/>
<display
value="1558 - Essential mixed cryoglobulinaemia - histologically proven"/>
</concept>
<concept>
<code value="prd1543"/>
<display
value="1543 - Essential mixed cryoglobulinaemia - no histology"/>
</concept>
<concept>
<code value="prd3230"/>
<display value="3230 - Fabry disease - histologically proven"/>
</concept>
<concept>
<code value="prd3224"/>
<display value="3224 - Fabry disease - no histology"/>
</concept>
<concept>
<code value="prd2545"/>
<display
value="2545 - Familial amyloid secondary to protein mutations - histologically proven"/>
</concept>
<concept>
<code value="prd2532"/>
<display
value="2532 - Familial amyloid secondary to protein mutations - no histology"/>
</concept>
<concept>
<code value="prd1308"/>
<display
value="1308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven"/>
</concept>
<concept>
<code value="prd1298"/>
<display
value="1298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology"/>
</concept>
<concept>
<code value="prd1280"/>
<display
value="1280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven"/>
</concept>
<concept>
<code value="prd1279"/>
<display
value="1279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology"/>
</concept>
<concept>
<code value="prd2668"/>
<display value="2668 - Familial haemolytic uraemic syndrome (HUS)"/>
</concept>
<concept>
<code value="prd3173"/>
<display value="3173 - Familial hypercalciuric hypocalcaemia"/>
</concept>
<concept>
<code value="prd3160"/>
<display value="3160 - Familial hypocalciuric hypercalcaemia"/>
</concept>
<concept>
<code value="prd3187"/>
<display value="3187 - Familial hypomagnesaemia"/>
</concept>
<concept>
<code value="prd1144"/>
<display
value="1144 - Familial IgA nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd1137"/>
<display value="1137 - Familial IgA nephropathy - no histology"/>
</concept>
<concept>
<code value="prd1911"/>
<display
value="1911 - Familial interstitial nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd1907"/>
<display
value="1907 - Familial interstitial nephropathy - no histology"/>
</concept>
<concept>
<code value="prd3379"/>
<display value="3379 - Familial nephropathy"/>
</concept>
<concept>
<code value="prd1618"/>
<display value="1618 - Familial reflux nephropathy"/>
</concept>
<concept>
<code value="prd2675"/>
<display
value="2675 - Familial thrombotic thrombocytopenic purpura(2675)"/>
</concept>
<concept>
<code value="prd2566"/>
<display
value="2566 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven"/>
</concept>
<concept>
<code value="prd2550"/>
<display
value="2550 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology"/>
</concept>
<concept>
<code value="prd2453"/>
<display value="2453 - Fibromuscular dysplasia of renal artery"/>
</concept>
<concept>
<code value="prd1354"/>
<display
value="1354 - Focal and segmental proliferative glomerulonephritis"/>
</concept>
<concept>
<code value="prd3754"/>
<display
value="3754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV "/>
</concept>
<concept>
<code value="prd3765"/>
<display
value="3765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium "/>
</concept>
<concept>
<code value="prd1320"/>
<display
value="1320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven"/>
</concept>
<concept>
<code value="prd1312"/>
<display
value="1312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology"/>
</concept>
<concept>
<code value="prd3777"/>
<display
value="3777 - Focal segmental glomerulosclerosis secondary to sickle cell"/>
</concept>
<concept>
<code value="prd3314"/>
<display value="3314 - Frasier syndrome"/>
</concept>
<concept>
<code value="prd3092"/>
<display value="3092 - Gitelman syndrome"/>
</concept>
<concept>
<code value="prd1656"/>
<display value="1656 - Glomerulocystic disease"/>
</concept>
<concept>
<code value="prd1377"/>
<display
value="1377 - Glomerulonephritis - histologically indeterminate"/>
</concept>
<concept>
<code value="prd3749"/>
<display value="3749 - Glomerulonephritis - no histology"/>
</concept>
<concept>
<code value="prd1365"/>
<display
value="1365 - Glomerulonephritis - secondary to systemic disease"/>
</concept>
<concept>
<code value="prd3125"/>
<display
value="3125 - Glucocorticoid suppressible hyperaldosteronism"/>
</concept>
<concept>
<code value="prd1417"/>
<display
value="1417 - Granulomatosis with polyangiitis - histologically proven"/>
</concept>
<concept>
<code value="prd1401"/>
<display
value="1401 - Granulomatosis with polyangiitis - no histology"/>
</concept>
<concept>
<code value="prd3572"/>
<display value="3572 - Haematuria and proteinuria - no histology"/>
</concept>
<concept>
<code value="prd2610"/>
<display
value="2610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associated"/>
</concept>
<concept>
<code value="prd2647"/>
<display
value="2647 - Haemolytic uraemic syndrome (HUS) secondary to systemic disease"/>
</concept>
<concept>
<code value="prd2257"/>
<display value="2257 - Hantavirus nephropathy"/>
</concept>
<concept>
<code value="prd1515"/>
<display
value="1515 - Henoch-Schönlein purpura / nephritis - histologically proven"/>
</concept>
<concept>
<code value="prd1504"/>
<display
value="1504 - Henoch-Schönlein purpura / nephritis - no histology"/>
</concept>
<concept>
<code value="prd2495"/>
<display value="2495 - Hepatorenal syndrome"/>
</concept>
<concept>
<code value="prd3305"/>
<display value="3305 - Horse-shoe kidney"/>
</concept>
<concept>
<code value="prd3662"/>
<display value="3662 - Hypercalcaemic nephropathy"/>
</concept>
<concept>
<code value="prd2993"/>
<display
value="2993 - Hypophosphataemic rickets autosomal recessive (AR)"/>
</concept>
<concept>
<code value="prd2986"/>
<display value="2986 - Hypophosphataemic rickets X-linked (XL)"/>
</concept>
<concept>
<code value="prd1251"/>
<display
value="1251 - Idiopathic rapidly progressive (crescentic) glomerulonephritis"/>
</concept>
<concept>
<code value="prd1813"/>
<display value="1813 - Idiopathic retroperitoneal fibrosis"/>
</concept>
<concept>
<code value="prd1128"/>
<display value="1128 - IgA nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd1116"/>
<display value="1116 - IgA nephropathy - no histology"/>
</concept>
<concept>
<code value="prd1163"/>
<display
value="1163 - IgA nephropathy secondary to liver cirrhosis - histologically proven"/>
</concept>
<concept>
<code value="prd1159"/>
<display
value="1159 - IgA nephropathy secondary to liver cirrhosis - no histology"/>
</concept>
<concept>
<code value="prd1171"/>
<display value="1171 - IgM - associated nephropathy"/>
</concept>
<concept>
<code value="prd2606"/>
<display value="2606 - Immunotactoid / fibrillary nephropathy"/>
</concept>
<concept>
<code value="prd3823"/>
<display
value="3823 - Infiltration by lymphoma - histologically proven"/>
</concept>
<concept>
<code value="prd3139"/>
<display
value="3139 - Inherited / genetic diabetes mellitus type II"/>
</concept>
<concept>
<code value="prd2940"/>
<display value="2940 - Inherited aminoaciduria"/>
</concept>
<concept>
<code value="prd2972"/>
<display value="2972 - Inherited renal glycosuria"/>
</concept>
<concept>
<code value="prd2407"/>
<display value="2407 - Ischaemic nephropathy - no histology"/>
</concept>
<concept>
<code value="prd2411"/>
<display
value="2411 - Ischaemic nephropathy / microvascular disease - histologically proven"/>
</concept>
<concept>
<code value="prd3712"/>
<display value="3712 - Isolated haematuria - no histology"/>
</concept>
<concept>
<code value="prd3720"/>
<display value="3720 - Isolated proteinuria - no histology"/>
</concept>
<concept>
<code value="prd3810"/>
<display value="3810 - Kidney stones due to ARPT deficiency"/>
</concept>
<concept>
<code value="prd3461"/>
<display value="3461 - Kidney tumour"/>
</concept>
<concept>
<code value="prd3351"/>
<display value="3351 - Lawrence-Moon-Biedl / Bardet-Biedl syndrome"/>
</concept>
<concept>
<code value="prd2177"/>
<display
value="2177 - Lead induced nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2165"/>
<display value="2165 - Lead induced nephropathy - no histology"/>
</concept>
<concept>
<code value="prd2242"/>
<display value="2242 - Leptospirosis"/>
</concept>
<concept>
<code value="prd3059"/>
<display
value="3059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency"/>
</concept>
<concept>
<code value="prd3102"/>
<display value="3102 - Liddle syndrome"/>
</concept>
<concept>
<code value="prd2597"/>
<display value="2597 - Light chain deposition disease"/>
</concept>
<concept>
<code value="prd2938"/>
<display value="2938 - Lowe syndrome (oculocerebrorenal syndrome)"/>
</concept>
<concept>
<code value="prd1866"/>
<display
value="1866 - Magnesium ammonium phosphate (struvite) urolithiasis"/>
</concept>
<concept>
<code value="prd2385"/>
<display
value="2385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2371"/>
<display
value="2371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology"/>
</concept>
<concept>
<code value="prd2804"/>
<display value="2804 - Medullary cystic kidney disease type I"/>
</concept>
<concept>
<code value="prd2815"/>
<display value="2815 - Medullary cystic kidney disease type II"/>
</concept>
<concept>
<code value="prd3295"/>
<display value="3295 - Medullary sponge kidneys"/>
</concept>
<concept>
<code value="prd1723"/>
<display value="1723 - Megacystis-megaureter"/>
</concept>
<concept>
<code value="prd1205"/>
<display value="1205 - Membranous nephropathy - drug induced"/>
</concept>
<concept>
<code value="prd1185"/>
<display value="1185 - Membranous nephropathy - idiopathic"/>
</concept>
<concept>
<code value="prd1214"/>
<display
value="1214 - Membranous nephropathy - infection associated"/>
</concept>
<concept>
<code value="prd1192"/>
<display
value="1192 - Membranous nephropathy - malignancy associated"/>
</concept>
<concept>
<code value="prd1349"/>
<display value="1349 - Mesangial proliferative glomerulonephritis "/>
</concept>
<concept>
<code value="prd1222"/>
<display value="1222 - Mesangiocapillary glomerulonephritis type 1"/>
</concept>
<concept>
<code value="prd1233"/>
<display
value="1233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)"/>
</concept>
<concept>
<code value="prd1246"/>
<display value="1246 - Mesangiocapillary glomerulonephritis type 3"/>
</concept>
<concept>
<code value="prd3501"/>
<display value="3501 - Mesoblastic nephroma - histologically proven"/>
</concept>
<concept>
<code value="prd1429"/>
<display
value="1429 - Microscopic polyangiitis - histologically proven"/>
</concept>
<concept>
<code value="prd1100"/>
<display
value="1100 - Minimal change nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd1090"/>
<display value="1090 - Minimal change nephropathy - no histology"/>
</concept>
<concept>
<code value="prd3367"/>
<display value="3367 - Mitochondrial cytopathy"/>
</concept>
<concept>
<code value="prd1639"/>
<display value="1639 - Multicystic dysplastic kidneys"/>
</concept>
<concept>
<code value="prd2584"/>
<display
value="2584 - Myeloma cast nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2578"/>
<display value="2578 - Myeloma kidney - no histology"/>
</concept>
<concept>
<code value="prd3253"/>
<display value="3253 - Nail-patella syndrome"/>
</concept>
<concept>
<code value="prd3044"/>
<display value="3044 - Nephrogenic diabetes insipidus"/>
</concept>
<concept>
<code value="prd2836"/>
<display value="2836 - Nephronophthisis"/>
</concept>
<concept>
<code value="prd2843"/>
<display value="2843 - Nephronophthisis - type 1 (juvenile type)"/>
</concept>
<concept>
<code value="prd2858"/>
<display value="2858 - Nephronophthisis - type 2 (infantile type)"/>
</concept>
<concept>
<code value="prd2862"/>
<display value="2862 - Nephronophthisis - type 3 (adolescent type)"/>
</concept>
<concept>
<code value="prd2870"/>
<display value="2870 - Nephronophthisis - type 4 (juvenile type)"/>
</concept>
<concept>
<code value="prd2889"/>
<display value="2889 - Nephronophthisis - type 5"/>
</concept>
<concept>
<code value="prd2891"/>
<display value="2891 - Nephronophthisis - type 6"/>
</concept>
<concept>
<code value="prd2098"/>
<display
value="2098 - Nephropathy due to aminoglycosides - histologically proven"/>
</concept>
<concept>
<code value="prd2080"/>
<display
value="2080 - Nephropathy due to aminoglycosides - no histology"/>
</concept>
<concept>
<code value="prd2112"/>
<display
value="2112 - Nephropathy due to amphotericin - histologically proven"/>
</concept>
<concept>
<code value="prd2108"/>
<display
value="2108 - Nephropathy due to amphotericin - no histology"/>
</concept>
<concept>
<code value="prd2033"/>
<display
value="2033 - Nephropathy due to analgesic drugs - histologically proven"/>
</concept>
<concept>
<code value="prd2022"/>
<display
value="2022 - Nephropathy due to analgesic drugs - no histology"/>
</concept>
<concept>
<code value="prd2051"/>
<display
value="2051 - Nephropathy due to ciclosporin - histologically proven"/>
</concept>
<concept>
<code value="prd2046"/>
<display
value="2046 - Nephropathy due to ciclosporin - no histology"/>
</concept>
<concept>
<code value="prd2131"/>
<display
value="2131 - Nephropathy due to cisplatin - histologically proven"/>
</concept>
<concept>
<code value="prd2120"/>
<display value="2120 - Nephropathy due to cisplatin - no histology"/>
</concept>
<concept>
<code value="prd2681"/>
<display value="2681 - Nephropathy due to eclampsia"/>
</concept>
<concept>
<code value="prd2154"/>
<display
value="2154 - Nephropathy due to lithium - histologically proven"/>
</concept>
<concept>
<code value="prd2149"/>
<display value="2149 - Nephropathy due to lithium - no histology"/>
</concept>
<concept>
<code value="prd3834"/>
<display value="3834 - Nephropathy due to pre-eclampsia"/>
</concept>
<concept>
<code value="prd2079"/>
<display
value="2079 - Nephropathy due to tacrolimus - histologically proven"/>
</concept>
<concept>
<code value="prd2067"/>
<display value="2067 - Nephropathy due to tacrolimus - no histology"/>
</concept>
<concept>
<code value="prd2288"/>
<display
value="2288 - Nephropathy related to HIV - histologically proven"/>
</concept>
<concept>
<code value="prd2274"/>
<display value="2274 - Nephropathy related to HIV - no histology"/>
</concept>
<concept>
<code value="prd3615"/>
<display
value="3615 - Nephrotic syndrome of childhood - no trial of steroids - no histology"/>
</concept>
<concept>
<code value="prd3604"/>
<display
value="3604 - Nephrotic syndrome of childhood - steroid resistant - no histology"/>
</concept>
<concept>
<code value="prd1019"/>
<display
value="1019 - Nephrotic syndrome of childhood - steroid sensitive - no histology"/>
</concept>
<concept>
<code value="prd1799"/>
<display
value="1799 - Obstructive nephropathy due to bladder cancer"/>
</concept>
<concept>
<code value="prd1809"/>
<display
value="1809 - Obstructive nephropathy due to other malignancies"/>
</concept>
<concept>
<code value="prd1781"/>
<display
value="1781 - Obstructive nephropathy due to prostate cancer"/>
</concept>
<concept>
<code value="prd1775"/>
<display
value="1775 - Obstructive nephropathy due to prostatic hypertrophy"/>
</concept>
<concept>
<code value="prd1734"/>
<display value="1734 - Oligomeganephronia"/>
</concept>
<concept>
<code value="prd2300"/>
<display value="2300 - Other specific infection"/>
</concept>
<concept>
<code value="prd3063"/>
<display
value="3063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity"/>
</concept>
<concept>
<code value="prd1455"/>
<display value="1455 - Polyarteritis nodosa"/>
</concept>
<concept>
<code value="prd1687"/>
<display value="1687 - Posterior urethral valves"/>
</concept>
<concept>
<code value="prd2901"/>
<display value="2901 - Primary Fanconi syndrome"/>
</concept>
<concept>
<code value="prd1267"/>
<display
value="1267 - Primary focal segmental glomerulosclerosis (FSGS)"/>
</concept>
<concept>
<code value="prd3194"/>
<display value="3194 - Primary hyperoxaluria"/>
</concept>
<concept>
<code value="prd3207"/>
<display value="3207 - Primary hyperoxaluria type I"/>
</concept>
<concept>
<code value="prd3211"/>
<display value="3211 - Primary hyperoxaluria type II"/>
</concept>
<concept>
<code value="prd3731"/>
<display value="3731 - Primary hyperoxaluria type III"/>
</concept>
<concept>
<code value="prd1602"/>
<display value="1602 - Primary reflux nephropathy - sporadic"/>
</concept>
<concept>
<code value="prd3000"/>
<display value="3000 - Primary renal tubular acidosis (RTA)"/>
</concept>
<concept>
<code value="prd3016"/>
<display
value="3016 - Proximal renal tubular acidosis (RTA) - type II"/>
</concept>
<concept>
<code value="prd3141"/>
<display value="3141 - Pseudohypoaldosteronism type 1"/>
</concept>
<concept>
<code value="prd3156"/>
<display
value="3156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)"/>
</concept>
<concept>
<code value="prd2219"/>
<display value="2219 - Radiation nephritis"/>
</concept>
<concept>
<code value="prd2226"/>
<display value="2226 - Renal / perinephric abscess"/>
</concept>
<concept>
<code value="prd2509"/>
<display value="2509 - Renal amyloidosis"/>
</concept>
<concept>
<code value="prd2469"/>
<display value="2469 - Renal arterial thrombosis / occlusion"/>
</concept>
<concept>
<code value="prd2424"/>
<display value="2424 - Renal artery stenosis"/>
</concept>
<concept>
<code value="prd3474"/>
<display value="3474 - Renal cell carcinoma - histologically proven"/>
</concept>
<concept>
<code value="prd3658"/>
<display value="3658 - Renal coloboma syndrome"/>
</concept>
<concept>
<code value="prd3627"/>
<display value="3627 - Renal cysts and diabetes syndrome"/>
</concept>
<concept>
<code value="prd1641"/>
<display
value="1641 - Renal dysplasia due to fetal ACE-inhibitor exposure"/>
</concept>
<concept>
<code value="prd3691"/>
<display value="3691 - Renal failure"/>
</concept>
<concept>
<code value="prd1747"/>
<display value="1747 - Renal papillary necrosis"/>
</concept>
<concept>
<code value="prd3796"/>
<display
value="3796 - Renal papillary necrosis caused by analgesics"/>
</concept>
<concept>
<code value="prd3783"/>
<display value="3783 - Renal papillary necrosis caused by diabetes"/>
</concept>
<concept>
<code value="prd3806"/>
<display
value="3806 - Renal papillary necrosis caused by sickle cell"/>
</concept>
<concept>
<code value="prd1976"/>
<display value="1976 - Renal sarcoidosis - histologically proven"/>
</concept>
<concept>
<code value="prd1969"/>
<display value="1969 - Renal sarcoidosis - no histology"/>
</concept>
<concept>
<code value="prd1536"/>
<display
value="1536 - Renal scleroderma / systemic sclerosis - histologically proven"/>
</concept>
<concept>
<code value="prd1527"/>
<display
value="1527 - Renal scleroderma / systemic sclerosis - no histology"/>
</concept>
<concept>
<code value="prd2235"/>
<display value="2235 - Renal tuberculosis"/>
</concept>
<concept>
<code value="prd2476"/>
<display value="2476 - Renal vein thrombosis"/>
</concept>
<concept>
<code value="prd3689"/>
<display value="3689 - Retroperitoneal fibrosis secondary to drugs"/>
</concept>
<concept>
<code value="prd1821"/>
<display
value="1821 - Retroperitoneal fibrosis secondary to malignancies"/>
</concept>
<concept>
<code value="prd3670"/>
<display
value="3670 - Retroperitoneal fibrosis secondary to peri-aortitis"/>
</concept>
<concept>
<code value="prd3269"/>
<display value="3269 - Rubinstein-Taybi syndrome"/>
</concept>
<concept>
<code value="prd2290"/>
<display value="2290 - Schistosomiasis"/>
</concept>
<concept>
<code value="prd2702"/>
<display
value="2702 - Sickle cell nephropathy - histologically proven"/>
</concept>
<concept>
<code value="prd2699"/>
<display value="2699 - Sickle cell nephropathy - no histology"/>
</concept>
<concept>
<code value="prd3517"/>
<display value="3517 - Single kidney identified in adulthood"/>
</concept>
<concept>
<code value="prd1694"/>
<display
value="1694 - Syndrome of agenesis of abdominal muscles - prune belly syndrome"/>
</concept>
<concept>
<code value="prd1493"/>
<display
value="1493 - Systemic lupus erythematosus / nephritis - histologically proven"/>
</concept>
<concept>
<code value="prd1486"/>
<display
value="1486 - Systemic lupus erythematosus / nephritis - no histology"/>
</concept>
<concept>
<code value="prd1383"/>
<display
value="1383 - Systemic vasculitis - ANCA negative - histologically proven"/>
</concept>
<concept>
<code value="prd3847"/>
<display
value="3847 - Systemic vasculitis - ANCA negative - no histology"/>
</concept>
<concept>
<code value="prd3852"/>
<display
value="3852 - Systemic vasculitis - ANCA positive - histologically proven"/>
</concept>
<concept>
<code value="prd1396"/>
<display
value="1396 - Systemic vasculitis - ANCA positive - no histology"/>
</concept>
<concept>
<code value="prd2787"/>
<display value="2787 - Thin basement membrane disease"/>
</concept>
<concept>
<code value="prd2634"/>
<display value="2634 - Thrombotic thrombocytopenic purpura (TTP)"/>
</concept>
<concept>
<code value="prd3346"/>
<display value="3346 - Townes-Brocks syndrome"/>
</concept>
<concept>
<code value="prd3488"/>
<display
value="3488 - Transitional cell carcinoma - histologically proven"/>
</concept>
<concept>
<code value="prd3276"/>
<display value="3276 - Tuberous sclerosis"/>
</concept>
<concept>
<code value="prd2917"/>
<display
value="2917 - Tubular disorder as part of inherited metabolic diseases"/>
</concept>
<concept>
<code value="prd1897"/>
<display
value="1897 - Tubulointerstitial nephritis - histologically proven"/>
</concept>
<concept>
<code value="prd1884"/>
<display value="1884 - Tubulointerstitial nephritis - no histology"/>
</concept>
<concept>
<code value="prd1930"/>
<display
value="1930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically proven"/>
</concept>
<concept>
<code value="prd1924"/>
<display
value="1924 - Tubulointerstitial nephritis associated with autoimmune disease - no histology"/>
</concept>
<concept>
<code value="prd1953"/>
<display
value="1953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically proven"/>
</concept>
<concept>
<code value="prd1948"/>
<display
value="1948 - Tubulointerstitial nephritis with uveitis (TINU) - no histology"/>
</concept>
<concept>
<code value="prd1878"/>
<display value="1878 - Uric acid urolithiasis"/>
</concept>
<concept>
<code value="prd2827"/>
<display
value="2827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)"/>
</concept>
<concept>
<code value="prd3282"/>
<display value="3282 - Von Hippel-Lindau disease"/>
</concept>
<concept>
<code value="prd3333"/>
<display value="3333 - Williams syndrome"/>
</concept>
<concept>
<code value="prd3490"/>
<display value="3490 - Wilms tumour - histologically proven"/>
</concept>
<concept>
<code value="prd3248"/>
<display value="3248 - Xanthinuria"/>
</concept>
<concept>
<code value="prd2261"/>
<display value="2261 - Xanthogranulomatous pyelonephritis"/>
</concept>
</include>
</compose>
</ValueSet>