Search Ontology:
Human Disease
hypogonadotropic hypogonadism 23 with or without anosmia
- Term ID
- DOID:0090091
- Synonyms
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- 46,XY disorder of sex development due to LHB deficiency
- 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
- 46,XY DSD due to LHB deficiency
- 46,XY DSD due to luteinizing hormone subunit beta deficiency
- fertile eunuch syndrome
- leydig cell hypoplasia due to LHB deficiency
- Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
- Pasqualini syndrome
- Definition
- A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13. (2)
- References
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- ICD10CM:Q56.1
- MIM:228300
- ORDO:325448
- Ontology
- Human Disease ( DOID:0090091 )
- is a type of
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Zebrafish Models