Disease association ontology term - MONDO:0979229 - congenital myopathy 26
Term summary
ID
MONDO:0979229
Name
congenital myopathy 26
Ontology or CV name
Disease association
Parents
is_a
congenital myopathy
Annotation
Disease association
MONDO:0979229
-
congenital myopathy 26
References:
PB_REF:0000006
Genes:
atb2 (SPBC800.05c)
nda2 (SPBC16A3.15c)