Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4277013 | Autosomal hereditary disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 66691000077115 | affection héréditaire autosomique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 688861000077115 | affection héréditaire autosomique (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 746648015 | Autosomal hereditary disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal hereditary disorder | est un(e) (attribut) | maladie héréditaire | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| syndrome de Waardenburg (trouble) | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some | |
| Hartsfield syndrome | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some | |
| Short stature due to growth hormone secretagogue receptor deficiency | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some | |
| Genetic hyperferritinemia without iron overload | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some | |
| Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some | |
| Female infertility due to zona pellucida defect (disorder) | est un(e) (attribut) | True | Autosomal hereditary disorder | Inferred relationship | Some |
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This concept is not in any reference sets
FHIR