Hypogonadotropic Hypogonadism 12 With Or Without Anosmia
Disease ID: disease_node_17198
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E23.0, MIM:614841 |
|---|---|
| Subclassof | DOID_0050737, DOID_0090070 |
| Data Source | DOID |
| Synonyms | familial hypogonadotrophic eunuchoidism, familial idiopathic gonadotrpin deficiency |
| Doid Label | hypogonadotropic hypogonadism 12 with or without anosmia |
| Doid Description | A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17198 |
| Doid Id | DOID_0090072 |
| Label | Hypogonadotropic Hypogonadism 12 With Or Without Anosmia |
- Outgoing r'ship
SUBCLASS_OFto/from Hypogonadotropic Hypogonadism(ID:disease_node_17175) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)