Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3316399012 | Disorder of sex development with intellectual disability syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316400017 | Disorder of sex development with intellectual disability syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316401018 | Pseudohermaphroditism with intellectual disability syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316402013 | Verloes Gillerot Fryns syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3316403015 | A rare association of malformations described in only three patients including two siblings. The first patient had profound intellectual deficit and clinical features including short stature, coarse face, deep-set eyes, microphthalmia, large ears, gynoid obesity, imperforate anus, sacral spina bifida, pseudovaginal perineoscrotal hypospadias, persistence of Mullerian structures, and low gonadotrophin levels. His XY sibling was raised as a girl, was slightly mentally impaired and had microphthalmia and large ears and short stature. The third patient had severe hearing loss, ocular colobomata, hypogonadism of central origin, distinct craniofacial features and skeletal anomalies with cervical spina bifida, hyperkyphosis and thoracic deformity. All patients had a normal 46, XY karyotype. Inheritance could be either autosomal recessive or X-linked. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
941241000172112 | syndrome de Verloes-Gillerot-Fryns | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
975481000172115 | syndrome d'anomalie du développement sexuel-déficience intellectuelle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
897991000172117 | geslachtsontwikkelingsstoornis, intellectuele achterstand | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
972611000172116 | pseudohermafroditisme, intellectuele achterstand | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Disorder of sex development with intellectual disability syndrome (disorder) | Is a | Pseudohermaphroditism | true | Inferred relationship | Some | ||
Disorder of sex development with intellectual disability syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Disorder of sex development with intellectual disability syndrome (disorder) | Is a | retard mental | false | Inferred relationship | Some | ||
Disorder of sex development with intellectual disability syndrome (disorder) | Finding site | Genital structure | false | Inferred relationship | Some | 2 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Finding site | Genital structure | false | Inferred relationship | Some | 3 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 3 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Disorder of sex development with intellectual disability syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Finding site | Genital structure | true | Inferred relationship | Some | 1 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 2 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 3 | |
Disorder of sex development with intellectual disability syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets