OBO ID: DOID:0110791 |
Term Name: | hereditary spastic paraplegia 3A | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0110791 ) |
OTHER hereditary spastic paraplegia 3A PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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