Disease #05474 (MFM-8 (myopathy, myofibrillar, type 8 (MFM-8)), OMIM:617258)

Official abbreviation MFM-8
Name myopathy, myofibrillar, type 8 (MFM-8)
OMIM ID 617258
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PYROXD1
Associated tissues -
Disease features autosomal recessive
Remarks -