Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1223673015 | Vohwinkel's mutilating keratoderma | en | Synonym | Active | Case sensitive | SNOMED CT core |
41186015 | Mutilating keratoderma | en | Synonym | Active | Case insensitive | SNOMED CT core |
4589802013 | Keratoderma hereditarium mutilans | en | Synonym | Active | Case insensitive | SNOMED CT core |
4589803015 | Mutilating keratoderma of Vohwinkel | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4589804014 | Vohwinkel syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
754208012 | Mutilating keratoderma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Keratoderma hereditarium mutilans with ichthyosis syndrome | Is a | True | Mutilating keratoderma | Inferred relationship | Some | |
Autosomal dominant mutilating keratoderma | Is a | False | Mutilating keratoderma | Inferred relationship | Some | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | False | Mutilating keratoderma | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set