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Entry Name Description Category Pathway Gene
H01160 Schizencephaly ... between the inner and outer liquor spaces. Gray matter-lined clefts in the cerebral cortex and a range of neurological presentations are characteristic. Mutations in SIX3, SHH, and EMX2 have been reported. Congenital malformation SIX3 [HSA:6496] [KO:K19473]
SHH [HSA:6469] [KO:K11988]
EMX2 [HSA:2018] [KO:K09317]
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