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Disease Ontology Browser
hereditary spastic paraplegia 45 (DOID:0110797)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 45; autosomal recessive spastic paraplegia type 45; autosomal recessive spastic paraplegia type 65; SPG45; SPG65
Alt IDs: OMIM:613162, ICD10CM:G11.4, ORDO:320396
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.

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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last database update
MGI 6.24
The Jackson Laboratory