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Autosomal recessive spastic paraplegia type 69

MONDO:0018421

Also known as: SPG69

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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodegenerative disease (171) Central nervous system disorder (107) Neuromuscular disease (106) Paraplegia (44) Palsy (33) Syndromic disease (25) Hereditary spastic paraplegia (23)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.