Disease #05787 (MFM7 (myopathy, myofibrillar, type 7 (MFM7)), OMIM:617114)

Official abbreviation MFM7
Name myopathy, myofibrillar, type 7 (MFM7)
OMIM ID 617114
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KY
Associated tissues -
Disease features -
Remarks -