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Familial gestational hyperthyroidism
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Familial hyperthyroidism due to mutations in TSH receptor
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor

TSHR
(UniProt - OMIM)
 TSHR
(UniProt - OMIM)

COMMON
GENES 		TSHR


Citations in the biomedical literature:


Familial gestational hyperthyroidism
TSHR
Familial hyperthyroidism due to mutations in TSH receptor



Familial gestational hyperthyroidism
Familial hyperthyroidism due to mutations in TSH receptor

Synonym(s):
(no synonyms)

Synonym(s):
- Familial non-immune hyperthyroidism
- Resistance to thyroid stimulating hormone
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare renal disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.