Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3644025016 | Agenesis of corpus callosum and abnormal genitalia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644026015 | Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644027012 | Proud syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644028019 | Agenesis of corpus callosum and abnormal genitalia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644029010 | Proud Levine Carpenter syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644030017 | Corpus callosum agenesis, abnormal genitalia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644031018 | A rare genetic developmental defect during embryogenesis syndrome with characteristics of agenesis of the corpus callosum, mild to severe neurological manifestations (intellectual disability, developmental delay, epilepsy, dystonia), and urogenital anomalies (hypospadias, cryptorchidism, renal dysplasia, ambiguous genitalia). Additionally skeletal anomalies (limb contractures, scoliosis), dysmorphic facial features (large eyes, prominent supraorbital ridges, synophrys) and optic atrophy have been observed. The disease is caused by mutation in the ARX gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Agenesis of corpus callosum | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Genitourinary congenital anomalies | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Finding site | Structure of genitourinary system (body structure) | false | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Finding site | Entire corpus callosum | true | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Finding site | Structure of genitourinary system (body structure) | true | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Finding site | Entire corpus callosum | false | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Associated morphology | Agenesis (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
Agenesis of corpus callosum and abnormal genitalia syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Agenesis of corpus callosum and abnormal genitalia syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets