Details of Disease | DrugMAP

General Information of Disease (ID: DISIHJ7B)

Disease Name	Cardiomyopathy, familial hypertrophic, 28
Synonyms	cardiomyopathy, familial hypertrophic, 28; CMH28
Disease Hierarchy	DISQ89HN: Familial hypertrophic cardiomyopathy DISIHJ7B: Cardiomyopathy, familial hypertrophic, 28
Disease Identifiers	MONDO ID MONDO_0030317 UMLS CUI C5543616 OMIM ID 619402 MedGen ID 1779612

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
FHOD3	OT1WUBQX	Strong	Autosomal dominant	[1]
------------------------------------------------------------------------------------

References

1	Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.