Hereditary spastic paraplegia 38

Definition

A hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15.

Also known as autosomal dominant spastic paraplegia type 38, hereditary spastic paraplegia type 38, SPG38 — per MONDO

Also identified as

• DOID 0110789 per MONDO
• MESH C567349 per MONDO
• OMIM 612335 per MONDO
• Orphanet 171617 per MONDO
• UMLS C2676732 per MONDO