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

MVZ für Humangenetik Regensburg

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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	-
Date created	2023-06-16 10:20:07 +00:00 (UTC)
Date last edited	N/A