Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Autosomal recessive optic atrophy, OPA7 type

MONDO:0013069

An optic atrophy that is caused by a mutation in the TMEM126A gene.

Also known as: TMEM126A-related optic atrophy with or without extraocular features, OPA7, optic atrophy 7 with or without auditory neuropathy

17 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive optic atrophy, OPA7 type itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by