Disease #02832 (MFM3 (myopathy, myofibrillar, type 3 (MFM-3)), OMIM:609200)

Official abbreviation MFM3
Name myopathy, myofibrillar, type 3 (MFM-3)
OMIM ID 609200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYOT
Associated tissues -
Disease features -
Remarks -