Agent Commons Collaborative Research

Hereditary spastic paraplegia 49

rare

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

Identifiers
MONDO:0014016 OMIM:615031Orphanet:320385
Causal genes
TECPR2
Part of
Complex hereditary spastic paraplegiaHereditary sensory and autonomic neuropathy
Also known as
autosomal recessive spastic paraplegia type 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

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