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Disease Ontology Browser
hereditary spastic paraplegia 90A (DOID:0070459)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 90A; SPG90A
Alt IDs: OMIM:620416
Definition: A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in heterozygous mutation in the SPTSSA gene on chromosome 14q13.1.

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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12/10/2024
MGI 6.24 		The Jackson Laboratory