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 |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | survenue (attribut) | congénital | 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) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | morphologie associée (attribut) | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | Autosomal dominant ichthyosis (disorder) | true | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | Erythrokeratodermia variabilis | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | Entire skin | true | Inferred relationship | Some | 1 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | peau de la région palmaire de la main (structure corporelle) | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | interprète (attribut) | Keratinization, function (observable entity) | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | Skin structure of sole of foot | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | interprète (attribut) | Keratinization, function (observable entity) | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | morphologie associée (attribut) | Hyperkeratosis | true | Inferred relationship | Some | 5 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | peau de la région palmaire de la main (structure corporelle) | true | Inferred relationship | Some | 5 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | morphologie associée (attribut) | Hyperkeratosis | true | Inferred relationship | Some | 6 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | Skin structure of sole of foot | true | Inferred relationship | Some | 6 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | Mutilating keratoderma | true | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | interprète (attribut) | Hearing, function (observable entity) | true | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | a pour interprétation (attribut) | altéré | true | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | structure du système auditif | true | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | Congenital keratoderma | true | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | ichtyose congénitale | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est un(e) (attribut) | Autosomal dominant mutilating keratoderma | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | est défini par la manifestation de (attribut) | Abnormal keratinisation | false | Inferred relationship | Some | ||
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 3 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | morphologie associée (attribut) | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 4 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | interprète (attribut) | Keratinization, function (observable entity) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets