Catalog

Autosomal recessive spastic paraplegia type 23

No MMS code

Link to WHO Definition

Autosomal recessive spastic paraplegia type 23 – http://id.who.int/icd/entity/1595722974

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.