Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a2

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Subtype of: Congenital muscular dystrophy due to dystroglycanopathy · Muscular dystrophy · Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2
MONDO_0013154
POMT2 Unknown
15894594 16701995 17559086 17634419 17878207 17923109 19138766 19299310 22700954 22958903 27421908 27604308 28815891
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a2.
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 impaired intellectual development), type b2 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.