Disease #00130 (CMH9 (CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9), OMIM:613765)

Official abbreviation CMH9
Name CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
OMIM ID 613765
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TTN
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.