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Optic atrophy 11

MONDO:0015011

Any autosomal recessive isolated optic atrophy in which the cause of the disease is a mutation in the YME1L1 gene.

Also known as: OPA11, YME1L1 autosomal recessive isolated optic atrophy, autosomal recessive isolated optic atrophy caused by mutation in YME1L1, optic atrophy 11, optic atrophy type 11

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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