Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1771706016 | Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1782790010 | Autosomal recessive keratitis-ichthyosis-deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1787870017 | Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | morphologie associée (attribut) | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | interprète (attribut) | Keratinization, function (observable entity) | true | Inferred relationship | Some | 2 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | Entire skin | true | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | structure du système auditif | true | Inferred relationship | Some | 3 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 4 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | morphologie associée (attribut) | dysplasie | true | Inferred relationship | Some | 4 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | Ectoderm structure | true | Inferred relationship | Some | 4 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | interprète (attribut) | Hearing, function (observable entity) | true | Inferred relationship | Some | 5 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | est un(e) (attribut) | Autosomal recessive ichthyosis (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | est un(e) (attribut) | Keratitis ichthyosis and deafness syndrome | true | Inferred relationship | Some | ||
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | morphologie associée (attribut) | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | Structure of skin region | false | Inferred relationship | Some | ||
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | morphologie associée (attribut) | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 2 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets