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Disease Ontology Browser
hereditary spastic paraplegia 79A (DOID:0070455)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 79A; SPG79A
Alt IDs: OMIM:620221
Definition: A hereditary spastic paraplegia characterized by slowly progressive cerebellar or sensory ataxia and spasticity of the lower limbs that has_material_basis_in heterozygous mutation in the UCHL1 gene on chromosome 4p13.

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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory