Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3780615017 | Moynahan syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3780616016 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3780617013 | Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3780618015 | A rare genetic epilepsy syndrome with characteristics of congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Epilepsy | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | morphologie associée (attribut) | Congenital absence | false | Inferred relationship | Some | 1 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | localisation d'une constatation (attribut) | structure du cerveau | true | Inferred relationship | Some | 2 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | localisation d'une constatation (attribut) | Hair structure (body structure) | true | Inferred relationship | Some | 1 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Congenital alopecia | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Intellectual disability | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Alopecia, epilepsy, intellectual disability syndrome Moynahan type | morphologie associée (attribut) | Absence (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets