Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b3

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Congenital muscular dystrophy · Congenital muscular dystrophy due to dystroglycanopathy · Muscular dystrophy
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3
MONDO_0013155
POMGNT1 Unknown
11709191 12588800
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b3.
5 View disease cluster →
Myopathy caused by variation in POMGNT1 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Congenital muscular dystrophy due to dystroglycanopathy 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Muscle eye brain disease 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Walker-warburg syndrome 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1.