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hereditary spastic paraplegia 90B (DOID:0070460)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 90B; SPG90B
Alt IDs: OMIM:620417
Definition: A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous 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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12/17/2024
MGI 6.24 		The Jackson Laboratory