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Disease Ontology Browser
hereditary spastic paraplegia 5A (DOID:0110810)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 5A; autosomal recessive spastic paraplegia type 5A; SPG5A
Alt IDs: OMIM:270800, ICD10CM:G11.4, ORDO:100986
Definition: A hereditary spastic paraplegia that is characterized by progressive muscle weakness and paraplegia and has_material_basis_in mutation in the CYP7B1 gene on chromosome 8q12.

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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MGI 6.20
The Jackson Laboratory