Search Result

 Top
1 to 2 of 2
Entry Name Description Category Pathway Gene
H01657 Nephrotic syndrome Nephrotic syndrome (NPHS) is a heterogeneous group of disorders characterized by heavy proteinuria (more than 3.5 grams per day), hypoalbuminemia, hyperlipidemia, and edema. Congenital nephrotic syndrome ... Urinary system disease (NPHS1) NPHS1 [HSA:4868] [KO:K24496]
(NPHS2) NPHS2 [HSA:7827] [KO:K18268]
(NPHS3) PLCE1 [HSA:51196] [KO:K05860]
(NPHS4) WT1 [HSA:7490] [KO:K09234]
(NPHS5) LAMB2 [HSA:3913] [KO:K06243]
(NPHS6) PTPRO [HSA:5800] [KO:K18035]
(NPHS7) DGKE [HSA:8526] [KO:K00901]
(NPHS8) ARHGDIA [HSA:396] [KO:K12462]
(NPHS9) COQ8B [HSA:79934] [KO:K08869]
(NPHS10) EMP2 [HSA:2013] [KO:K26256]
(NPHS11) NUP107 [HSA:57122] [KO:K14301]
(NPHS12) NUP93 [HSA:9688] [KO:K14309]
(NPHS13) NUP205 [HSA:23165] [KO:K14310]
(NPHS14) SGPL1 [HSA:8879] [KO:K01634]
(NPHS15) MAGI2 [HSA:9863] [KO:K05629]
(NPHS16) KANK2 [HSA:25959] [KO:K22808]
(NPHS17) NUP85 [HSA:79902] [KO:K14304]
(NPHS18) NUP133 [HSA:55746] [KO:K14300]
(NPHS19) NUP160 [HSA:23279] [KO:K14303]
(NPHS20) TBC1D8B [HSA:54885] [KO:K19951]
(NPHS21/25) AVIL [HSA:10677] [KO:K08017]
(NPHS22) NOS1AP [HSA:9722] [KO:K16513]
(NPHS23) KIRREL1 [HSA:55243] [KO:K25874]
(NPHS24) DAAM2 [HSA:23500] [KO:K04512]
(NPHS26) LAMA5 [HSA:3911] [KO:K06240]
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]
1 to 2 of 2
[ KEGG | DISEASE | DRUG | MEDICUS ]