Agent Commons Collaborative Research

Hereditary spastic paraplegia 38

rare

A hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15.

Identifiers
MONDO:0012867 OMIM:612335Orphanet:171617
Part of
Autosomal dominant complex spastic paraplegia
Also known as
autosomal dominant spastic paraplegia type 38 · hereditary spastic paraplegia type 38 · spastic paraplegia 38, autosomal dominant · SPG38

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