You are using an outdated browser. Please upgrade your browser to improve your experience.

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

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Uniprot Description An autosomal recessive disorder characterized by congenital muscular dystrophy associated with mental retardation and mild structural brain abnormalities.
Mondo Term and Equivalent IDs
MONDO:0013159:  muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
UMLS:C3150415: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found