Disease association ontology term - MONDO:0013159 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

Term summary

ID: MONDO:0013159
Name: muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
Ontology or CV name: Disease association

Parents

is_a muscular dystrophy-dystroglycanopathy, type B
is_a myopathy caused by variation in POMT1

Annotation

Disease association

MONDO:0013159 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

References:

PB_REF:0000006

Genes:

ogm4 (SPBC16C6.09)