Hereditary spastic paraplegia 13

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the HSPD1 gene.

Also known as hereditary spastic paraplegia caused by mutation in HSPD1, hereditary spastic paraplegia type 13, HSPD1 hereditary spastic paraplegia, SPG13 — per MONDO

Also identified as

• DOID 0110766 per MONDO
• MESH C537485 per MONDO
• OMIM 605280 per MONDO
• Orphanet 100994 per MONDO
• UMLS C1854467 per MONDO