Details of Disease | DrugMAP

General Information of Disease (ID: DISW7D4A)

Disease Name	Congenital heart defects, multiple types, 7
Synonyms	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 7; CHTD7
Disease Hierarchy	DISYKSRF: Genetic disease DISW7D4A: Congenital heart defects, multiple types, 7
Disease Identifiers	MONDO ID MONDO_0032913 UMLS CUI C5394062 OMIM ID 618780 MedGen ID 1714491

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
FLT4	TTDCBX5	Strong	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
FLT4	OTRAA26B	Strong	Autosomal dominant	[1]
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References

1	Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. Nat Genet. 2017 Nov;49(11):1593-1601. doi: 10.1038/ng.3970. Epub 2017 Oct 9.