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 |
| 1223673015 | Vohwinkel's mutilating keratoderma | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 41186015 | Mutilating keratoderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4589802013 | Keratoderma hereditarium mutilans | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4589803015 | Mutilating keratoderma of Vohwinkel | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4589804014 | Vohwinkel syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 754208012 | Mutilating keratoderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | True | Mutilating keratoderma | Inferred relationship | Some | |
| Autosomal dominant mutilating keratoderma | est un(e) (attribut) | False | Mutilating keratoderma | Inferred relationship | Some | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) | est un(e) (attribut) | False | Mutilating keratoderma | Inferred relationship | Some |
Reference Sets
FHIR