Disease association ontology term - MONDO:0957224 - congenital myopathy 21 with early respiratory failure

Term summary

ID: MONDO:0957224
Name: congenital myopathy 21 with early respiratory failure
Ontology or CV name: Disease association

Parents

is_a congenital myopathy
is_a hereditary skeletal muscle disorder

Annotation

Disease association

MONDO:0957224 - congenital myopathy 21 with early respiratory failure

References:

PB_REF:0000006

Genes:

psi1 (SPCC830.07c)