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Disease Ontology Browser
hereditary spastic paraplegia 38 (DOID:0110789)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 38; autosomal dominant spastic paraplegia type 38; SPG38
Alt IDs: OMIM:612335, ICD10CM:G11.4, ORDO:171617
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.


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
10/10/2017
MGI 6.10
The Jackson Laboratory