0.1.0 - ci-build
0.1.0 - ci-build
SEMedicalAlertInformationImplementationGuide, published by HL7 Sweden. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7Sweden/hl7.fhir.r4.ig.medicalalertinformation/ and changes regularly. See the Directory of published versions
| Official URL: http://hl7.se/fhir/r4/ig/medicalalertinformation/ValueSet/59821000052101 | Version: 0.1.0 | |||
| Draft as of 2026-01-16 | Computable Name: SEAlertInformationMedicalConditionSnomedVS | |||
References
http://snomed.info/sct version Not Stated (use latest from terminology server)| Code | Display |
| 41291007 | angioödem |
| 9651007 | långt QT-syndrom |
| 70995007 | pulmonell hypertoni |
| 373662000 | primär binjurebarksinsufficiens |
| 405501007 | malign hypertermi |
| 64779008 | blodkoagulationssjukdom |
| 53891000052101 | trombocytrelaterad sjukdom med ökad blödningstendens |
| 126729006 | trombotisk mikroangiopati |
| 234467004 | trombofili |
| 91637004 | myasthenia gravis |
| 234422006 | akut intermittent porfyri |
| 58275005 | porphyria variegata |
| 7425008 | hereditär koproporfyri |
| 64081000 | brist på porfobilinogensyntetas |
| 360631004 | brist på kolinesteras 2, ospecifik |
| 33211000 | komplikation till anestesi |
| 718447001 | svår intubation |
| 707147002 | aspleni |
| 31323000 | svår kombinerad immunbrist |
| 17182001 | agranulocytos |
| 770942003 | Kostmanns syndrom |
| 89454001 | Shwachmans syndrom |
| 203551000052109 | störning av neutrofilfunktion |
| 439784005 | kirurgiskt anlagd arteriovenös fistel |
| 27718001 | Maple syrup urine disease |
| 116020001 | rubbning i omsättningen av förgrenade aminosyror |
| 39929009 | rubbning i fettsyraomsättningen |
| 7046009 | hyperleucin-isoleucinemi |
| 87827003 | brist på isovaleryl-CoA-dehydrogenas |
| 42393006 | metylmalonisk acidemi |
| 69080001 | brist på propionyl-CoA-karboxylas |
| 1156591005 | fettsyreoxidationsdefekt |
| 82319005 | brist på acyl-CoA-dehydrogenas |
| 36444000 | rubbning i ureaomsättningscykeln |
| 237929000 | rubbning i lysin- och hydroxilysinomsättningen |
| 41013004 | brist på argininosuccinatlyas |
| 398680004 | citrullinemi |
| 29633007 | glykogeninlagringssjukdom |
| 39452003 | rubbning i fruktosomsättningen |
| 190760009 | rubbningar i pyruvatomsättningen och glukoneogenesen |
| 75934005 | ämnesomsättningssjukdom |
| 238006008 | rubbning i purin- och pyrimidinomsättningen |
| 16851005 | mitokondriell myopati |
| 237751000 | kongenital adrenal hyperplasi |
| 737315000 | enterokolit utlöst av födoämnesprotein |
| 439218000 | kirurgiskt anlagt arteriovenöst graft |
Expansion from tx.fhir.org based on SNOMED CT International edition 01-Feb 2025
This value set contains 44 concepts
| System | Code | Display (en) | JSON | XML |
http://snomed.info/sct | 41291007 | Angioedema | ||
http://snomed.info/sct | 9651007 | Long QT syndrome | ||
http://snomed.info/sct | 70995007 | Pulmonary hypertension | ||
http://snomed.info/sct | 373662000 | Primary adrenocortical insufficiency (disorder) | ||
http://snomed.info/sct | 405501007 | Malignant hyperthermia | ||
http://snomed.info/sct | 64779008 | Blood coagulation disorder | ||
http://snomed.info/sct | 126729006 | Thrombotic microangiopathy | ||
http://snomed.info/sct | 234467004 | Thrombophilia | ||
http://snomed.info/sct | 91637004 | Myasthenia gravis | ||
http://snomed.info/sct | 234422006 | Acute intermittent porphyria | ||
http://snomed.info/sct | 58275005 | Variegate porphyria | ||
http://snomed.info/sct | 7425008 | Hereditary coproporphyria | ||
http://snomed.info/sct | 64081000 | Porphobilinogen synthase deficiency | ||
http://snomed.info/sct | 360631004 | Deficiency of choline esterase II (unspecific) | ||
http://snomed.info/sct | 33211000 | Complication of anesthesia | ||
http://snomed.info/sct | 718447001 | Difficult intubation | ||
http://snomed.info/sct | 707147002 | Asplenia (disorder) | ||
http://snomed.info/sct | 31323000 | Severe combined immunodeficiency disease | ||
http://snomed.info/sct | 17182001 | Agranulocytosis | ||
http://snomed.info/sct | 770942003 | Severe congenital neutropenia type 3 | ||
http://snomed.info/sct | 89454001 | Shwachman syndrome | ||
http://snomed.info/sct | 439784005 | Surgically constructed arteriovenous fistula (finding) | ||
http://snomed.info/sct | 27718001 | Maple syrup urine disease | ||
http://snomed.info/sct | 116020001 | Disorder of branched-chain amino acid metabolism | ||
http://snomed.info/sct | 39929009 | Disorder of fatty acid metabolism | ||
http://snomed.info/sct | 7046009 | Hyperleucine-isoleucinemia | ||
http://snomed.info/sct | 87827003 | Isovaleryl-CoA dehydrogenase deficiency | ||
http://snomed.info/sct | 42393006 | Methylmalonic acidemia | ||
http://snomed.info/sct | 69080001 | Propionic acidemia | ||
http://snomed.info/sct | 1156591005 | Fatty acid oxidation defect (disorder) | ||
http://snomed.info/sct | 82319005 | Acyl-CoA dehydrogenase deficiency | ||
http://snomed.info/sct | 36444000 | Disorder of the urea cycle metabolism | ||
http://snomed.info/sct | 237929000 | Disorder of lysine and hydroxylysine metabolism | ||
http://snomed.info/sct | 41013004 | Argininosuccinate lyase deficiency | ||
http://snomed.info/sct | 398680004 | Citrullinemia (disorder) | ||
http://snomed.info/sct | 29633007 | Glycogen storage disease | ||
http://snomed.info/sct | 39452003 | Disorder of fructose metabolism | ||
http://snomed.info/sct | 190760009 | Disorders of pyruvate metabolism and gluconeogenesis | ||
http://snomed.info/sct | 75934005 | Metabolic disease | ||
http://snomed.info/sct | 238006008 | Disorder of purine and pyrimidine metabolism | ||
http://snomed.info/sct | 16851005 | Mitochondrial myopathy | ||
http://snomed.info/sct | 237751000 | Congenital adrenal hyperplasia | ||
http://snomed.info/sct | 737315000 | Allergic enterocolitis caused by food protein | ||
http://snomed.info/sct | 439218000 | Surgically constructed arteriovenous graft (finding) |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |