Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary peripheral neuropathy · Inherited dystonia · Autosomal recessive syndromic cerebellar ataxia
Ataxia - oculomotor apraxia type 4
Any oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.
This condition has no sub-types.