Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b2

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Subtype of: Congenital muscular dystrophy due to dystroglycanopathy · Muscular dystrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2
  • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B2
MONDO_0013160
POMT2 Unknown
15894594 16701995 17559086 17634419 17878207 17923109 19138766 19299310 27421908 27604308
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b2.
5 View disease cluster →
Myopathy caused by variation in POMT2 1 shared genePOMT2 Related via 1 shared gene including POMT2. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a2 1 shared genePOMT2 Related via 1 shared gene including POMT2. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared genePOMT2 Related via 1 shared gene including POMT2. Muscle eye brain disease 1 shared genePOMT2 Related via 1 shared gene including POMT2. Walker-warburg syndrome 1 shared genePOMT2 Related via 1 shared gene including POMT2.