Autosomal recessive complex spastic paraplegia type 9B

Definition

Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.

Also known as ALDH18A1 autosomal recessive complex spastic paraplegia, AR-SPG9B, autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1, hereditary spastic paraplegia type 9B, SPG9B — per MONDO

Also identified as

• DOID 0110825 per MONDO
• OMIM 616586 per MONDO
• Orphanet 447760 per MONDO
• UMLS C5568980 per MONDO