Ataxia - oculomotor apraxia type 4

MONDO:0014557

Any oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.

Also known as: AOA4, PNKP oculomotor apraxia or related oculomotor disease, ataxia - oculomotor apraxia type 4, oculomotor apraxia or related oculomotor disease caused by mutation in PNKP, ataxia-oculomotor apraxia 4, ataxia-oculomotor apraxia-4

26 clinical trials for this condition and its sub-types, 0 tagged with Ataxia - oculomotor apraxia type 4 itself.

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Where it sits in the disease tree

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↑ Hereditary peripheral neuropathy (479) ↑ Inherited dystonia (36) ↑ Autosomal recessive syndromic cerebellar ataxia (2)

Including sub-types (26) Tagged with Ataxia - oculomotor apraxia type 4 (0)

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