Hypogonadotropic Hypogonadism 7 With Or Without Anosmia
Disease ID: disease_node_17192
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E23.0, MIM:146110 |
|---|---|
| Subclassof | DOID_0050737, DOID_0090070 |
| Data Source | DOID |
| Doid Label | hypogonadotropic hypogonadism 7 with or without anosmia |
| Doid Description | A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17192 |
| Doid Id | DOID_0090078 |
| Label | Hypogonadotropic Hypogonadism 7 With Or Without Anosmia |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hypogonadotropic Hypogonadism(ID:disease_node_17175) (Disease)