Hereditary spastic paraplegia 49

MONDO:0014016

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the TECPR2 gene.

Also known as: SPG49, TECPR2 hereditary spastic paraplegia, autosomal recessive spastic paraplegia type 49, hereditary spastic paraplegia 49, hereditary spastic paraplegia caused by mutation in TECPR2, hereditary spastic paraplegia type 49, neuropathy, hereditary sensory and autonomic, type IX, with developmental delay, spastic paraplegia 49, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 49 itself.

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↑ Complex hereditary spastic paraplegia (7)

Including sub-types (2) Tagged with Hereditary spastic paraplegia 49 (0)

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