Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308613015 | Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308614014 | Keratoderma hereditarium mutilans with ichthyosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308615010 | Camisa disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308616011 | Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308617019 | Vohwinkel ichthyosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308618012 | A diffuse palmoplantar keratoderma with manifestation of honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness.Follows an autosomal dominant mode of transmission. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3854491000052114 | syndrom med keratoderma hereditarium mutilans och iktyos | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | Congenital ichthyosis of skin | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | autosomalt dominant mutilerande keratodermi | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Associated morphology | utvecklingsabnormitet | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 2 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | Autosomal dominant ichthyosis (disorder) | true | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | Erythrokeratodermia variabilis | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Interprets | Keratinization | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure of sole of foot (body structure) | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Interprets | Keratinization | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 5 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 5 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 6 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Skin structure of sole of foot (body structure) | true | Inferred relationship | Some | 6 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | Mutilating keratoderma | true | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | Congenital keratoderma | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets