All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05684 neuropathy, optic neuropathy, optic - - 159 157 ACO2, DNM1L, MFN2, NR2F1, OPA1, RTN4IP1, SPG7, SSBP1 - -
04293 OPA atrophy, optic (OPA) - - 648 598 ACO2, DNM1L, OPA1, OPA3, RTN4IP1, SSBP1, TMEM126A, YME1L1 - -
05194 OPA-10 atrophy, optic, type 10, with or without ataxia, mental retardation, and seizures (OPA-10) 616732 - 0 1 RTN4IP1 eyes -
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