Hereditary spastic paraplegia 8

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the WASHC5 gene.

Also known as autosomal dominant spastic paraplegia type 8, hereditary spastic paraplegia caused by mutation in WASHC5, hereditary spastic paraplegia type 8, SPG8, WASHC5 hereditary spastic paraplegia — per MONDO

Also identified as

• DOID 0110823 per MONDO
• MESH C580458 per MONDO
• OMIM 603563 per MONDO
• Orphanet 100989 per MONDO
• UMLS C1863704 per MONDO