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Entry Name Description Category Pathway Gene
H00557 Cutis laxa Cutis laxa is a heterogeneous group of connective tissue disorders with variable organ involvement. The most obvious symptom of cutis laxa is loose and sagging skin due to reduced elastic fibers in the ... Congenital malformation (ADCL1) ELN [HSA:2006] [KO:K14211]
(ADCL2/ARCL1A) FBLN5 [HSA:10516] [KO:K17340]
(ADCL3/ARCL3A) ALDH18A1 [HSA:5832] [KO:K12657]
(ARCL1B) EFEMP2 [HSA:30008] [KO:K19866]
(ARCL1C) LTBP4 [HSA:8425] [KO:K08023]
(ARCL1D) EFEMP1 [HSA:2202] [KO:K18262]
(ARCL2A/WSS) ATP6V0A2 [HSA:23545] [KO:K02154]
(ARCL2B/ARCL3B) PYCR1 [HSA:5831] [KO:K00286]
(ARCL2C) ATP6V1E1 [HSA:529] [KO:K02150]
(ARCL2D) ATP6V1A [HSA:523] [KO:K02145]
(ARCL2E) LTBP1 [HSA:4052] [KO:K19559]
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]
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