Disease association ontology term - MONDO:0014140 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

Term summary

ID: MONDO:0014140
Name: muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
Ontology or CV name: Disease association

Parents

is_a muscular dystrophy-dystroglycanopathy, type A
is_a muscle-eye-brain disease
is_a myopathy caused by variation in GMPPB

Annotation

Disease association

MONDO:0014140 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

References:

PB_REF:0000006

Genes:

mpg1 (SPCC1906.01)