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DHDDS-related syndrome
MONDO:1010097Any neurological disorder in which the cause of the disease is a mutation in the DHDDS gene.
Also known as: progressive myoclonus ataxia
0 clinical trials for this condition and its sub-types, 0 tagged with DHDDS-related syndrome itself.
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Browse by category →Sub-types of DHDDS-related syndrome
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Retinitis pigmentosa 59 0 trials
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