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 -
Date created 2023-06-16 10:18:49 +00:00 (UTC)
Date last edited 2023-06-16 10:24:04 +00:00 (UTC)

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