Disease association ontology term - MONDO:0859264 - congenital myopathy 11
Term summary
ID
MONDO:0859264
Name
congenital myopathy 11
Ontology or CV name
Disease association
Parents
is_a
congenital myopathy
is_a
hereditary skeletal muscle disorder
Annotation
Disease association
MONDO:0859264
-
congenital myopathy 11
References:
PB_REF:0000006
Genes:
phs1 (SPBC19C2.15c)