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Disease Ontology Browser
hereditary spastic paraplegia 57 (DOID:0110809)
Synonyms: autosomal recessive spastic paraplegia 57; autosomal recessive spastic paraplegia type 57; SPG57
Alt IDs: OMIM:615658, ICD10CM:G11.4, ORDO:431329
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12.


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
03/21/2017
MGI 6.08
The Jackson Laboratory