ODCs

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Familial gestational hyperthyroidism

1 OMIM reference -
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

Familial gestational hyperthyroidism

Leydig cell hypoplasia due to complete LH resistance

TSHR

(UniProt - OMIM)

LHCGR

(UniProt - OMIM)


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

Citations in the biomedical literature:

Familial gestational hyperthyroidism		Leydig cell hypoplasia due to complete LH resistance
	Synonym(s): (no synonyms)		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 circulatory system disease - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare infertility - Rare urogenital disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.