Disease #00154 (CMH4 (CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4), OMIM:115197)

Official abbreviation CMH4
Name CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4
OMIM ID 115197
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MYBPC3
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 09:22:12 +00:00 (UTC)
Date last edited N/A

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