Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771704018 | X-linked dominant chondrodysplasia punctata of Happle (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1782788014 | X-linked dominant chondrodysplasia punctata of Happle | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1787869018 | X-linked dominant ichthyosis (Happle) | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | dysplasie | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | X-linked hereditary disease | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | Developmental hereditary disorder | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | affection dégénérative du système musculosquelettique | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | Atrophoderma (disorder) | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | Congenital anomaly of skin | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | est un(e) (attribut) | Chondrodysplasia punctata | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | atrophie (anomalie morphologique) | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | localisation d'une constatation (attribut) | structure osseuse | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | localisation d'une constatation (attribut) | structure osseuse | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | atrophie (anomalie morphologique) | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 3 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | localisation d'une constatation (attribut) | structure osseuse | false | Inferred relationship | Some | 3 | |
| X-linked dominant chondrodysplasia punctata of Happle (disorder) | morphologie associée (attribut) | Congenital dysplasia | false | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR