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hereditary spastic paraplegia 3A
Summary
- Synonym
-
- FSP1
- SPG3A
- autosomal dominant familial spastic paraplegia 1
- autosomal dominant spastic paraplegia 3
- autosomal dominant spastic paraplegia type 3
- strumpell disease
- Definition
- A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.
- Super Class
- autosomal dominant disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110791
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
