Disease association ontology term - MONDO:0032852 - myopathy, congenital, with structured cores and z-line abnormalities

Term summary

ID: MONDO:0032852
Name: myopathy, congenital, with structured cores and z-line abnormalities
Ontology or CV name: Disease association

Parents

is_a congenital myopathy
is_a ACTN2-related cardiac and skeletal myopathy

Annotation

Disease association

MONDO:0032852 - myopathy, congenital, with structured cores and z-line abnormalities

References:

PB_REF:0000006

Genes:

ain1 (SPAC15A10.08)