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Entry | Name | Description | Category | Pathway | Gene |
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H01012 | Oculo-auricular syndrome | ... ocular abnormalities include bilateral microcornea, posterior synechiae, cataract, chorioretinal colobomas, and rod-cone dystrophy. Mutation in the human Hmx1 ortholog HMX1 (NKX5-3) results in this disease. | Congenital malformation | HMX1 [HSA:3166] [KO:K09349] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |