All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04293 OPA atrophy, optic (OPA) - - 1065 966 ACO2, DNM1L, OPA1, OPA3, RTN4IP1, SSBP1, TMEM126A, YME1L1 - -
03222 OPA7 atrophy, optic, type 7, with/without auditory neuropathy (OPA-7) 612989 AR - - TMEM126A - -
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