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Entry Name Description Category Pathway Gene
H01885 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome
MPPH syndrome
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH) is rare overgrowth disorder. MCAP [DS:H02153] and MPPH show very similar symptoms; the main symptoms are progressive megalencephaly ... Congenital malformation (MPPH1) PIK3R2 [HSA:5296] [KO:K02649]
(MPPH2) AKT3 [HSA:10000] [KO:K04456]
(MPPH3) CCND2 [HSA:894] [KO:K10151]
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