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Entry Name Description Category Pathway Gene
H01722 Galloway-Mowat syndrome Galloway-Mowat Syndrome (GAMOS) is an autosomal recessively inherited condition characterized by the association of nephrotic syndrome and central nervous system involvement. Several case reports and studies ... Congenital malformation (GAMOS1) WDR73 [HSA:84942]
(GAMOS2) LAGE3 [HSA:8270] [KO:K15902]
(GAMOS3) OSGEP [HSA:55644] [KO:K01409]
(GAMOS4) TP53RK [HSA:112858] [KO:K08851]
(GAMOS5) TPRKB [HSA:51002] [KO:K15901]
(GAMOS6) WDR4 [HSA:10785] [KO:K15443]
(GAMOS7) NUP107 [HSA:57122] [KO:K14301]
(GAMOS8) NUP133 [HSA:55746] [KO:K14300]
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