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Hypogonadotropic hypogonadism 23 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the LHB gene.
- Identifiers
- MONDO:0009223 OMIM:228300Orphanet:325448
- Causal genes
- LHB
- Also known as
- 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 · eunuchoidism with spermatogenesis, normal FSH and low or normal interstitial cell-stimulating hormone (ICSH)
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