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Hereditary optic atrophy

MONDO:0043878

A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.

Also known as: hereditary optic atrophy, Atrophies, hereditary optic, atrophy, hereditary optic, hereditary optic Atrophies, optic atrophy, hereditary

38 clinical trials for this condition and its sub-types.

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Sub-types

Leber hereditary optic neuropathy (17) Autosomal dominant optic atrophy (5) Autosomal dominant optic atrophy, classic form (3) Optic atrophy 6 (1) ACO2-related optic atrophy with or without extraocular features (0) Al Gazali Khidr Prem Chandran syndrome (0) Autosomal dominant optic atrophy and peripheral neuropathy (0) Autosomal dominant optic atrophy plus syndrome (0) Autosomal recessive optic atrophy, OPA7 type (0) Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome (0) Leber optic atrophy and dystonia (0) Optic atrophy 10 with or without ataxia, intellectual disability, and seizures (0) Optic atrophy 11 (0) Optic atrophy 12 (0) Optic atrophy 13 with retinal and foveal abnormalities (0) Optic atrophy 14 (0) Optic atrophy 15 (0) Optic atrophy 16 (0) Optic atrophy 2 (0) Optic atrophy 3 (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Central nervous system disorder (97) Optic nerve disorder (19) Human disease (14) Inherited neurodegenerative disorder (10) Hereditary neurological disease (5) Optic atrophy (4)
Trials to join now! 14 Not yet recruiting 3 Not yet finished but already full! 9 Completed 11 Terminated 1
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