Disease association ontology term - MONDO:0033556 - muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15

Term summary

ID: MONDO:0033556
Name: muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
Ontology or CV name: Disease association

Parents

is_a muscular dystrophy-dystroglycanopathy, type B
is_a DPM3-congenital disorder of glycosylation

Annotation

Disease association

MONDO:0033556 - muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15

References:

PB_REF:0000006

Genes:

dpm3 (SPBC1677.02)