Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
41186015 | Mutilating keratoderma | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
754208012 | Mutilating keratoderma (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
1223673015 | Vohwinkel's mutilating keratoderma | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
4589802013 | Keratoderma hereditarium mutilans | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
4589803015 | Mutilating keratoderma of Vohwinkel | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
4589804014 | Vohwinkel syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal dominant mutilating keratoderma | Is a | False | Mutilating keratoderma | Inferred relationship | Existential restriction modifier | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | False | Mutilating keratoderma | Inferred relationship | Existential restriction modifier | |
Keratoderma hereditarium mutilans with ichthyosis syndrome | Is a | True | Mutilating keratoderma | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets