Disease association ontology term - MONDO:0009708 - myopathy, myosin storage, autosomal recessive
Term summary
ID
MONDO:0009708
Name
myopathy, myosin storage, autosomal recessive
Ontology or CV name
Disease association
Parents
excluded_subClassOf
hyaline body myopathy
is_a
congenital myopathy
is_a
hereditary skeletal muscle disorder
Annotation
Disease association
MONDO:0009708
-
myopathy, myosin storage, autosomal recessive
References:
PB_REF:0000006
Genes:
myo2 (SPCC645.05c)
myp2 (SPAC4A8.05c)