| Metadata | |
|---|---|
| ID | DOID:0110791 |
| Name | hereditary spastic paraplegia 3A |
| 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. https://www.ncbi.nlm.nih.gov/pubmed/11685207 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant familial spastic paraplegia 1 [EXACT] autosomal dominant spastic paraplegia 3 [EXACT] autosomal dominant spastic paraplegia type 3 [EXACT] FSP1 [EXACT] SPG3A [EXACT] strumpell disease [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance has symptom some muscle weakness |