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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] [KO:K24754] (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] (GAMOS9) GON7 [HSA:84520] [KO:K15903] (GAMOS10) YRDC [HSA:79693] [KO:K07566] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |