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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 hyperthyroidism due to mutations in TSH receptor
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 hyperthyroidism due to mutations in TSH receptor
TSHR
Leydig cell hypoplasia due to partial LH resistance
LHCGR



Familial hyperthyroidism due to mutations in TSH receptor
Leydig cell hypoplasia due to partial LH resistance

Synonym(s):
- Familial non-immune hyperthyroidism
- Resistance to thyroid stimulating hormone

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 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:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
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.