Autosomal recessive spastic paraplegia type 23 (Q99390): Difference between revisions

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Latest revision as of 16:03, 16 August 2026

Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.

Language	Label	Description	Also known as
default for all languages	ID_1595722974
English	Autosomal recessive spastic paraplegia type 23	Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.