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Disease Ontology Browser
hereditary spastic paraplegia 70 (DOID:0070454)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 70; SPG70
Alt IDs: OMIM:620323
Definition: A hereditary spastic paraplegia characterized by infantile onset of motor delay and difficulties walking due to spasticity of the lower limbs that has_material_basis_in compound heterozygous mutation in the MARS1 gene on chromosome 12q13.3.

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