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Optic atrophy 13 with retinal and foveal abnormalities

MONDO:0008135

Also known as: optic atrophy 13 with retinal and foveal abnormalities, optic atrophy with negative Electroretinograms

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

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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 optic atrophy (6) Hereditary neurological disease (5)
Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 3 Completed 5 Terminated 1
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