Hereditary spastic paraplegia 11

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene.

Also known as autosomal recessive spastic paraplegia type 11, hereditary spastic paraplegia caused by mutation in SPG11, hereditary spastic paraplegia type 11, HSP-TCC, Nakamura-Osame syndrome, spastic paraplegia-intellectual disability-thin corpus callosum syndrome, SPG11, SPG11 hereditary spastic paraplegia — per MONDO

Also identified as

• DOID 0110764 per MONDO
• NCIT C148317 per MONDO
• OMIM 604360 per MONDO
• Orphanet 2822 per MONDO
• SCTID 715491000 per MONDO
• UMLS C1858479 per MONDO

Affected Organs