Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:613151 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3; MDDGB3

Xenbase Genes: pomgnt1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013155 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
MONDO:0018277 - obsolete congenital muscular dystrophy with cerebellar involvement

Disease Ontology (DO):
DOID:0112378 - muscular dystrophy-dystroglycanopathy type B3