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Disease Ontology Browser
hereditary spastic paraplegia 3A (DOID:0110791)
Alliance: disease page
Synonyms: autosomal dominant familial spastic paraplegia 1; autosomal dominant spastic paraplegia 3; autosomal dominant spastic paraplegia type 3; FSP1; SPG3A; strumpell disease
Alt IDs: OMIM:182600, ICD10CM:G11.4, ORDO:100984
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory