Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a4

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Subtype of: Congenital muscular dystrophy · 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, 4
MONDO_0000171MONDO_0009678
FKTN Causal
9690476 10545611 12601708 14627679 17034757 17036286 17044012 17878207 18177472 19179078 19342235 20961758 21228398 22958903 24530477 27421908 27604308 30220444
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a4.
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Myopathy caused by variation in FKTN 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type b4 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared geneFKTN Related via 1 shared gene including FKTN. Muscle eye brain disease 1 shared geneFKTN Related via 1 shared gene including FKTN. Walker-warburg syndrome 1 shared geneFKTN Related via 1 shared gene including FKTN.