Disease #00131 (CMYP5 (CONGENITAL MYOPATHY 5 WITH CARDIOMYOPATHY), OMIM:611705)

Official abbreviation CMYP5
Name CONGENITAL MYOPATHY 5 WITH CARDIOMYOPATHY
OMIM ID 611705
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TTN
Associated tissues -
Disease features -
Remarks -

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