Autosomal dominant optic atrophy
MONDO:0020250An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss.
Also known as: ADOA, DOA, optic atrophy, autosomal dominant, dominant optic atrophy
30 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal dominant optic atrophy, classic form
(3)
Al Gazali Khidr Prem Chandran syndrome
(0)
Autosomal dominant optic atrophy and peripheral neuropathy
(0)
Autosomal dominant optic atrophy plus syndrome
(0)
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
(0)
Optic atrophy 3
(0)
Optic atrophy 5
(0)
Optic atrophy 8
(0)
Optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant
(0)
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
(0)