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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02041 | Myopia | Myopia is the most common ocular disorder worldwide, and high myopia in particular is one of the leading causes of blindness. Nonsyndromic, high myopia is highly heritable, and to date a few causative ... | Nervous system disease |
(MYP6) SCO2 [HSA:9997] [KO:K23755] (MYP21) ZNF644 [HSA:84146] [KO:K24374] (MYP22) PRIMPOL [HSA:201973] [KO:K22761] (MYP23) LRPAP1 [HSA:4043] [KO:K22290] (MYP24) SLC39A5 [HSA:283375] [KO:K14711] (MYP25) P4HA2 [HSA:8974] [KO:K00472] (MYP26) ARR3 [HSA:407] [KO:K13801] (MYP27) CPSF1 [HSA:29894] [KO:K14401] (MYP28) LOXL3 [HSA:84695] [KO:K00280] (MCVD) P3H2 [HSA:55214] [KO:K22459] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |