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Familial gestational hyperthyroidism
1 OMIM reference -
1 associated gene
28 connected diseases
No signs/symptoms info
Disease Type of connection
Familial hyperthyroidism due to mutations in TSH receptor
Hypothyroidism due to TSH receptor mutations
Thyroid hypoplasia
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Autosomal dominant hyper-IgE syndrome
Fibronectin glomerulopathy
Budd-Chiari syndrome
Familial thrombocytosis
Polycythemia vera
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Spondylocarpotarsal synostosis
Auriculocondylar syndrome
Autosomal agammaglobulinemia
Autosomal dominant hypocalcemia
Early infantile epileptic encephalopathy
Familial hypocalciuric hypercalcemia type 2
Familial male-limited precocious puberty
Familial multiple nevi flammei
Isolated thyroid-stimulating hormone deficiency
Leydig cell hypoplasia due to complete LH resistance
Leydig cell hypoplasia due to partial LH resistance
SHORT syndrome
Sturge-Weber syndrome
(no synonyms)

Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare renal disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
TSHR P16473603372
No signs/symptoms info available.