Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
377013019 | Abnormality of neurogenesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
643850015 | Abnormality of neurogenesis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5068871000241115 | anomalie de neurogénèse | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Atelencephaly | Is a | False | Abnormality of neurogenesis | Inferred relationship | Some | |
Aprosencephaly | Is a | False | Abnormality of neurogenesis | Inferred relationship | Some | |
microcéphalie | Is a | False | Abnormality of neurogenesis | Inferred relationship | Some | |
A group of rare central nervous system malformations characterized by varying degrees of absence or dysplasia of the derivatives of the prosencephalon (i.e. telencephalon and diencephalon), with an intact cranial vault. The spectrum comprises atelencephaly, the less severe form, in which only the telencephalon is affected, and aprosencephaly, where the diencephalon is also involved. The malformations may occur in an isolated form or in association with other anomalies. | Is a | True | Abnormality of neurogenesis | Inferred relationship | Some |
This concept is not in any reference sets