Disease association ontology term - MONDO:0034109 - congenital myopathy with reduced type 2 muscle fibers

Term summary

ID: MONDO:0034109
Name: congenital myopathy with reduced type 2 muscle fibers
Ontology or CV name: Disease association

Parents

is_a autosomal recessive disease
is_a congenital myopathy

Annotation

Disease association

MONDO:0034109 - congenital myopathy with reduced type 2 muscle fibers

References:

PB_REF:0000006

Genes:

cdc4 (SPAP8A3.08)