Disease #01555 (SPMM (myopathy, scapuloperoneal, MYH7-related (SPMM)), OMIM:181430)

Official abbreviation SPMM
Name myopathy, scapuloperoneal, MYH7-related (SPMM)
OMIM ID 181430
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYH7
Associated tissues -
Disease features -
Remarks -