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Disease Ontology Browser
hereditary spastic paraplegia 37 (DOID:0110788)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 37; autosomal dominant spastic paraplegia type 37; SPG37
Alt IDs: OMIM:611945, ICD10CM:G11.4, ORDO:171612
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory