Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1196418013 | Congenital anomaly of endocrine testis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1209826012 | Congenital anomaly of endocrine testis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5854101000241118 | anomalie congénitale du testicule endocrine | 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 |
Congenital absence of germinal epithelium of testes (disorder) | Is a | False | Congenital anomaly of endocrine testis (disorder) | Inferred relationship | Some | |
Congenital absence of both testes (disorder) | Is a | False | Congenital anomaly of endocrine testis (disorder) | Inferred relationship | Some | |
Leydig cell agenesis | Is a | True | Congenital anomaly of endocrine testis (disorder) | Inferred relationship | Some | |
Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, early development of secondary sexual characteristics and reduced adult height. | Is a | True | Congenital anomaly of endocrine testis (disorder) | Inferred relationship | Some |
This concept is not in any reference sets