Hereditary spastic paraplegia 3A

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene.

Also known as ATL1 hereditary spastic paraplegia, autosomal dominant spastic paraplegia type 3, FSP1, hereditary spastic paraplegia caused by mutation in ATL1, hereditary spastic paraplegia type 3A, spastic Paraplegia 3A, spastic paraplegia 3a, autosomal dominant, SPG3A, strumpell disease — per MONDO

Also identified as

• DOID 0110791 per MONDO
• MESH C536864 per MONDO
• NCIT C142893 per MONDO
• OMIM 182600 per MONDO
• Orphanet 100984 per MONDO
• UMLS C2931355 per MONDO

Affected Organs