Autosomal recessive spastic paraplegia type 78

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.

Also known as ATP13A2 hereditary spastic paraplegia, hereditary spastic paraplegia caused by mutation in ATP13A2, spastic paraplegia 78, autosomal recessive, spastic paraplegia 78, autosomal recessive; SPG78, SPG78 — per MONDO

Also identified as

• DOID 0112348 per MONDO
• OMIM 617225 per MONDO
• Orphanet 513436 per MONDO
• UMLS C5567893 per MONDO