Details of Disease | DrugMAP

General Information of Disease (ID: DIS0OC59)

Disease Name	Familial gestational hyperthyroidism
Synonyms	hyperthyroidism, familial gestational
Disease Hierarchy	DISYKSRF: Genetic disease DISX87ZH: Hyperthyroidism DIS5V7J6: Pregnancy disorder DIS0OC59: Familial gestational hyperthyroidism
Disease Identifiers	MONDO ID MONDO_0011309 MESH ID C566384 UMLS CUI C1863959 OMIM ID 603373 MedGen ID 355106 Orphanet ID 99819 SNOMED CT ID 703309000

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
TSHR	TT6NYJA	Limited	Genetic Variation	[1]
TSHR	TT6NYJA	Definitive	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
TSHR	OT0BC8LB	Definitive	Autosomal dominant	[1]
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References

1	Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin. N Engl J Med. 1998 Dec 17;339(25):1823-6. doi: 10.1056/NEJM199812173392505.