Disease association ontology term - MONDO:0800341 - congenital myopathy 4A, autosomal dominant

Term summary

ID: MONDO:0800341
Name: congenital myopathy 4A, autosomal dominant
Ontology or CV name: Disease association

Parents

excluded_subClassOf cap myopathy
is_a TPM3-related myopathy

Annotation

Disease association

MONDO:0800341 - congenital myopathy 4A, autosomal dominant

References:

PB_REF:0000006

Genes:

cdc8 (SPAC27F1.02c)