Spastic paraplegia 3, autosomal dominant [Supplementary Concept]
Hereditary autosomal dominant spastic paraplegia that is associated with mutations in the ATL1 gene. OMIM: 182600
Date introduced: August 25, 2010
MeSH Unique ID: C536864
Heading Mapped to:
Entry Terms:
- Spastic Paraplegia Type 3a
- Spastic Paraplegia 3
- Spastic Paraplegia 3a
- Spg3a
- Strumpell disease
- Familial spastic paraplegia, autosomal dominant, 1
- Fsp1 Familial spastic paraplegia 1
- SPG3A Spastic paraplegia 3a