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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01798 | Autosomal dominant neovascular inflammatory vitreoretinopathy | ... membranes (ERMs), and proliferative iris and retinal neovascularization. It is caused by mutations in CAPN5 gene, encoding an intracellular protease expressed in the retina. In most patients the diagnosis ... | Nervous system disease | CAPN5 [HSA:726] [KO:K08574] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |