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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial gestational hyperthyroidism
Leydig cell hypoplasia due to partial LH resistance

TSHR LHCGR


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Familial gestational hyperthyroidism
TSHR
Leydig cell hypoplasia due to partial LH resistance
LHCGR



Familial gestational hyperthyroidism
Leydig cell hypoplasia due to partial LH resistance

Synonym(s):
(no synonyms)

Synonym(s):
- 46,XY DSD due to partial LH receptor inactivation
- 46,XY DSD due to partial LH resistance
- 46,XY DSD due to partial luteinizing hormone resistance
- 46,XY disorder of sex developement due to partial LH receptor inactivation
- 46,XY disorder of sex developement due to partial LH resistance
- 46,XY disorder of sex developement due to partial luteinizing hormone resistance
- Leydig cell hypoplasia due to partial LH receptor inactivation
- Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
- Leydig cell hypoplasia due to partial 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.