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/1.2.752.116.3.1.16.1.1 | Version: 0.1.0 | |||
| Draft as of 2025-08-26 | Computable Name: SEAlertInformationOtherMedicalConditionVS | |||
Uppmärksamhetsinformation för annat medicinskt tillstånd.
References
This value set includes codes based on the following rules:
Expansion from tx.fhir.org based on:
This value set contains 87 concepts
| Code | System | Display |
| T78.3 | http://hl7.org/fhir/sid/icd-10 | Angioneurotic oedema |
| I27.0 | http://hl7.org/fhir/sid/icd-10 | Primary pulmonary hypertension |
| I27.2 | http://hl7.org/fhir/sid/icd-10 | Other secondary pulmonary hypertension |
| E27.1 | http://hl7.org/fhir/sid/icd-10 | Primary adrenocortical insufficiency |
| T88.3 | http://hl7.org/fhir/sid/icd-10 | Malignant hyperthermia due to anaesthesia |
| D68.0 | http://hl7.org/fhir/sid/icd-10 | Von Willebrand disease |
| D68.1 | http://hl7.org/fhir/sid/icd-10 | Hereditary factor XI deficiency |
| D68.2 | http://hl7.org/fhir/sid/icd-10 | Hereditary deficiency of other clotting factors |
| D68.3 | http://hl7.org/fhir/sid/icd-10 | Haemorrhagic disorder due to circulating anticoagulants |
| D68.4 | http://hl7.org/fhir/sid/icd-10 | Acquired coagulation factor deficiency |
| D68.5 | http://hl7.org/fhir/sid/icd-10 | Primary thrombophilia |
| D68.6 | http://hl7.org/fhir/sid/icd-10 | Other thrombophilia |
| D68.8 | http://hl7.org/fhir/sid/icd-10 | Other specified coagulation defects |
| D68.9 | http://hl7.org/fhir/sid/icd-10 | Coagulation defect, unspecified |
| D69.0 | http://hl7.org/fhir/sid/icd-10 | Allergic purpura |
| D69.1 | http://hl7.org/fhir/sid/icd-10 | Qualitative platelet defects |
| D69.3 | http://hl7.org/fhir/sid/icd-10 | Idiopathic thrombocytopenic purpura |
| D69.4 | http://hl7.org/fhir/sid/icd-10 | Other primary thrombocytopenia |
| D69.5 | http://hl7.org/fhir/sid/icd-10 | Secondary thrombocytopenia |
| D69.6 | http://hl7.org/fhir/sid/icd-10 | Thrombocytopenia, unspecified |
| M31.1 | http://hl7.org/fhir/sid/icd-10 | Thrombotic microangiopathy |
| G70.0 | http://hl7.org/fhir/sid/icd-10 | Myasthenia gravis |
| E88.0 | http://hl7.org/fhir/sid/icd-10 | Disorders of plasma-protein metabolism, not elsewhere classified |
| T88.2 | http://hl7.org/fhir/sid/icd-10 | Shock due to anaesthesia |
| T88.5 | http://hl7.org/fhir/sid/icd-10 | Other complications of anaesthesia |
| T88.4 | http://hl7.org/fhir/sid/icd-10 | Failed or difficult intubation |
| D73.0 | http://hl7.org/fhir/sid/icd-10 | Hyposplenism |
| Q89.0 | http://hl7.org/fhir/sid/icd-10 | Congenital malformations of spleen |
| D81 | http://hl7.org/fhir/sid/icd-10 | Combined immunodeficiencies |
| I77.0 | http://hl7.org/fhir/sid/icd-10 | Arteriovenous fistula, acquired |
| E71.0 | http://hl7.org/fhir/sid/icd-10 | Maple-syrup-urine disease |
| E71.2 | http://hl7.org/fhir/sid/icd-10 | Disorder of branched-chain amino-acid metabolism, unspecified |
| E71.3 | http://hl7.org/fhir/sid/icd-10 | Disorders of fatty-acid metabolism |
| E72.2 | http://hl7.org/fhir/sid/icd-10 | Disorders of urea cycle metabolism |
| E72.3 | http://hl7.org/fhir/sid/icd-10 | Disorders of lysine and hydroxylysine metabolism |
| E74.0 | http://hl7.org/fhir/sid/icd-10 | Glycogen storage disease |
| E74.1 | http://hl7.org/fhir/sid/icd-10 | Disorders of fructose metabolism |
| E74.4 | http://hl7.org/fhir/sid/icd-10 | Disorders of pyruvate metabolism and gluconeogenesis |
| E88.9 | http://hl7.org/fhir/sid/icd-10 | Metabolic disorder, unspecified |
| E79.8 | http://hl7.org/fhir/sid/icd-10 | Other disorders of purine and pyrimidine metabolism |
| G71.3 | http://hl7.org/fhir/sid/icd-10 | Mitochondrial myopathy, not elsewhere classified |
| E25.0 | http://hl7.org/fhir/sid/icd-10 | Congenital adrenogenital disorders associated with enzyme deficiency |
| K52.2 | http://hl7.org/fhir/sid/icd-10 | Allergic and dietetic gastroenteritis and colitis |
| 41291007 | http://snomed.info/sct | Angioedema |
| 9651007 | http://snomed.info/sct | Long QT syndrome |
| 70995007 | http://snomed.info/sct | Pulmonary hypertension |
| 373662000 | http://snomed.info/sct | Primary adrenocortical insufficiency (disorder) |
| 405501007 | http://snomed.info/sct | malign hypertermi |
| 64779008 | http://snomed.info/sct | Blood coagulation disorder |
| 126729006 | http://snomed.info/sct | Thrombotic microangiopathy |
| 234467004 | http://snomed.info/sct | Thrombophilia |
| 91637004 | http://snomed.info/sct | Myasthenia gravis |
| 234422006 | http://snomed.info/sct | Acute intermittent porphyria |
| 58275005 | http://snomed.info/sct | Variegate porphyria |
| 7425008 | http://snomed.info/sct | Hereditary coproporphyria |
| 64081000 | http://snomed.info/sct | Porphobilinogen synthase deficiency |
| 360631004 | http://snomed.info/sct | Deficiency of choline esterase II (unspecific) |
| 33211000 | http://snomed.info/sct | Complication of anesthesia |
| 718447001 | http://snomed.info/sct | svår intubation |
| 707147002 | http://snomed.info/sct | Asplenia (disorder) |
| 31323000 | http://snomed.info/sct | Severe combined immunodeficiency disease |
| 17182001 | http://snomed.info/sct | Agranulocytosis |
| 770942003 | http://snomed.info/sct | Severe congenital neutropenia type 3 |
| 89454001 | http://snomed.info/sct | Shwachman syndrome |
| 439784005 | http://snomed.info/sct | Surgically constructed arteriovenous fistula (finding) |
| 27718001 | http://snomed.info/sct | Maple syrup urine disease |
| 116020001 | http://snomed.info/sct | Disorder of branched-chain amino acid metabolism |
| 39929009 | http://snomed.info/sct | Disorder of fatty acid metabolism |
| 7046009 | http://snomed.info/sct | Hyperleucine-isoleucinemia |
| 87827003 | http://snomed.info/sct | Isovaleryl-CoA dehydrogenase deficiency |
| 42393006 | http://snomed.info/sct | Methylmalonic acidemia |
| 69080001 | http://snomed.info/sct | Propionic acidemia |
| 1156591005 | http://snomed.info/sct | Fatty acid oxidation defect (disorder) |
| 82319005 | http://snomed.info/sct | Acyl-CoA dehydrogenase deficiency |
| 36444000 | http://snomed.info/sct | Disorder of the urea cycle metabolism |
| 237929000 | http://snomed.info/sct | Disorder of lysine and hydroxylysine metabolism |
| 41013004 | http://snomed.info/sct | Argininosuccinate lyase deficiency |
| 398680004 | http://snomed.info/sct | Citrullinemia (disorder) |
| 29633007 | http://snomed.info/sct | Glycogen storage disease |
| 39452003 | http://snomed.info/sct | rubbning i fruktosomsättningen |
| 190760009 | http://snomed.info/sct | Disorders of pyruvate metabolism and gluconeogenesis |
| 75934005 | http://snomed.info/sct | Metabolic disease |
| 238006008 | http://snomed.info/sct | Disorder of purine and pyrimidine metabolism |
| 16851005 | http://snomed.info/sct | Mitochondrial myopathy |
| 237751000 | http://snomed.info/sct | Congenital adrenal hyperplasia |
| 737315000 | http://snomed.info/sct | Allergic enterocolitis caused by food protein |
| 439218000 | http://snomed.info/sct | 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 |