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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00787 | Congenital stationary night blindness | Congenital stationary night blindness (CSNB) is a group of nonprogressive retinal disorders characterized by impaired night vision. CSNB is currently associated with X-linked genes (NYX, CACNA1F), autosomal ... | Nervous system disease |
(CSNB1A) NYX [HSA:60506] [KO:K08129] (CSNB1B) GRM6 [HSA:2916] [KO:K04608] (CSNB1C) TRPM1 [HSA:4308] [KO:K04976] (CSNB1D) SLC24A1 [HSA:9187] [KO:K13749] (CSNB1E) GPR179 [HSA:440435] [KO:K22961] (CSNB1F) LRIT3 [HSA:345193] [KO:K24491] (CSNB1H) GNB3 [HSA:2784] [KO:K07825] (CSNB1I) GUCY2D [HSA:3000] [KO:K12321] (CSNB2A) CACNA1F [HSA:778] [KO:K04853] (CSNB2B) CABP4 [HSA:57010] [KO:K23531] (CSNBAD1) RHO [HSA:6010] [KO:K04250] (CSNBAD2) PDE6B [HSA:5158] [KO:K13756] (CSNBAD3 CSNB1G) GNAT1 [HSA:2779] [KO:K04631] (CSNBO1) SAG [HSA:6295] [KO:K19627] (CSNBO2) GRK1 [HSA:6011] [KO:K00909] |
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| H01633 |
High blood pressure Hypertension |
High blood pressure (hypertension) is the most frequent classic cardiovascular risk factor and accounts for a large proportion of cardiovascular mortality, the main cause of death worldwide. Hypertension ... | Cardiovascular disease |
(EHT) PTGIS [HSA:5740] [KO:K01831] (EHT) AGTR1 [HSA:185] [KO:K04166] (EHT) ADD1 [HSA:118] [KO:K18622] (EHT) AGT [HSA:183] [KO:K09821] (EHT) ECE1 [HSA:1889] [KO:K01415] (EHT) CYP3A5 [HSA:1577] [KO:K17690] (EHT) NOS3 [HSA:4846] [KO:K13242] (EHT) GNB3 [HSA:2784] [KO:K07825] NR3C2 [HSA:4306] [KO:K08555] (GRA) CYP11B2 [HSA:1585] [KO:K07433] (GRA) CYP11B1 [HSA:1584] [KO:K00497] (AME) HSD11B2 [HSA:3291] [KO:K00071] (LIDLS) SCNN1B [HSA:6338] [KO:K04825] (LIDLS) SCNN1G [HSA:6340] [KO:K04827] (LIDLS) SCNN1A [HSA:6337] [KO:K04824] |
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