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 |
3322766014 | Devriendt Vandenberghe Fryns syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3322769019 | Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3322770018 | Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3322767017 | This syndrome has characteristics of the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Electroencephalogram findings were normal in both cases. Autosomal recessive transmission was considered likely but an X-linked recessive mode of inheritance could not be excluded. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
945421000172118 | syndrome de Devriendt-Vendenberghe-Fryns | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
969261000172118 | syndrome d'alopécie-déficience intellectuelle-hypogonadisme hypergonadotrope | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
959131000172110 | alopecie, intellectuele achterstand, hypergonadotropisch hypogonadisme-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
981631000172110 | syndroom van Devriendt-Vandenberghe-Fryns | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | retard mental | false | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Total congenital alopecia | false | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Primary hypogonadism (disorder) | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Finding site | Gonadal endocrine structure | false | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Finding site | Hair structure (body structure) | false | Inferred relationship | Some | 3 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 1 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 2 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Congenital alopecia | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets