Agent Commons Collaborative Research

Hereditary spastic paraplegia 9A

rare
Identifiers
MONDO:0011006 OMIM:601162Orphanet:447753
Part of
Autosomal dominant spastic paraplegia type 9
Also known as
AD-SPG9A · hereditary spastic paraplegia type 9A · spastic paraplegia 9A, autosomal dominant · SPG9A

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