hypogonadotropic hypogonadism 23 with or without anosmia (Q9390597)
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A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13.
- Hypogonadism with spermatogenesis
- PASQUALINI SYNDROME
- Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
- 46,XY disorder of sex development due to LHB deficiency
- 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
- leydig cell hypoplasia due to LHB deficiency
- 46,XY DSD due to luteinizing hormone subunit beta deficiency
- fertile eunuch syndrome
- 46,XY DSD due to LHB deficiency
- HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA
- HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23
- HH23
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypogonadotropic hypogonadism 23 with or without anosmia |
A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13. |
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Wikipedia(3 entries)
- dewiki Pasqualini-Syndrom
- enwiki Fertile eunuch syndrome
- plwiki Zespół płodnego eunucha