ODCs

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Leydig cell hypoplasia due to LHB deficiency

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Leydig cell hypoplasia due to complete LH resistance

1 OMIM reference -
1 associated gene
No signs/symptoms info

Leydig cell hypoplasia due to LHB deficiency

Leydig cell hypoplasia due to complete LH resistance

LHB

(UniProt - OMIM)

LHCGR

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LHB	(0.52)	LHCGR

Citations in the biomedical literature:

Leydig cell hypoplasia due to LHB deficiency		Leydig cell hypoplasia due to complete 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		Synonym(s): - 46,XY DSD due to complete LH receptor inactivation - 46,XY DSD due to complete LH resistance - 46,XY DSD due to complete luteinizing hormone receptor inactivation - 46,XY DSD due to complete luteinizing hormone resistance - 46,XY disorder of sex development due to complete LH receptor inactivation - 46,XY disorder of sex development due to complete LH resistance - 46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation - 46,XY disorder of sex development due to complete luteinizing hormone resistance - Leydig cel hypoplasia due to complete LH receptor inactivation - Leydig cel hypoplasia due to complete luteinizing hormone receptor inactivation - Leydig cel hypoplasia due to complete luteinizing hormone resistance

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare infertility - Rare urogenital disease		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 -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.