Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1770259012 | Familial psoriasis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1781492017 | Familial psoriasis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
305571000077114 | psoriasis familial | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial psoriasis with affected first degree relative (disorder) | Is a | True | Familial psoriasis (disorder) | Inferred relationship | Some | |
Familial psoriasis without affected first degree relative (disorder) | Is a | True | Familial psoriasis (disorder) | Inferred relationship | Some | |
A rare, X-linked syndromic intellectual disability disorder characterized by severe intellectual disability, psychomotor developmental delay, generalized seizures, and psoriasis. Mild craniofacial dysmorphism, such as hypertelorism, broad nasal bridge, anteverted nares, macrostomia, highly arched palate and large ears, is also associated. There have been no further descriptions in the literature since 1988. | Is a | True | Familial psoriasis (disorder) | Inferred relationship | Some |
This concept is not in any reference sets