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Leydig cell hypoplasia due to LHB deficiency
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Familial male-limited precocious puberty
Leydig cell hypoplasia due to complete LH resistance
Leydig cell hypoplasia due to partial LH resistance
Synonym(s):
- 46,XY DSD due to LHB deficiency
- 46,XY DSD 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 luteinizing hormone subunit beta deficiency
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare infertility
- Rare urogenital disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
LHB P01229152780
No signs/symptoms info available.