Disease association ontology term - MONDO:0014220 - myopathy due to myoadenylate deaminase deficiency

Term summary

ID: MONDO:0014220
Name: myopathy due to myoadenylate deaminase deficiency
Ontology or CV name: Disease association

Parents

excluded_subClassOf adenosine monophosphate deaminase deficiency
is_a myopathy
is_a hereditary skeletal muscle disorder

Annotation

Disease association

MONDO:0014220 - myopathy due to myoadenylate deaminase deficiency

References:

PB_REF:0000006

Genes:

ada1 (SPBC106.04)