Auditory neuropathy-optic atrophy syndrome

MONDO:0060582

A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is characterized by onset of visual and hearing impairment in the first or second decades.

Also known as: ANOA, auditory neuropathy and optic atrophy, multiple mitochondrial dysfunctions syndrome 9A

13 clinical trials for this condition and its sub-types, 0 tagged with Auditory neuropathy-optic atrophy syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (999) ↑ FDXR-related optic atrophy mitochondrial dysfunction syndrome (0)

Including sub-types (13) Tagged with Auditory neuropathy-optic atrophy syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.