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Disease Ontology Browser
hereditary spastic paraplegia 32 (DOID:0110783)
Synonyms: autosomal recessive spastic paraplegia 32; autosomal recessive spastic paraplegia type 32; SPG32
Alt IDs: OMIM:611252, ICD10CM:G11.4, ORDO:171622
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.


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
07/11/2017
MGI 6.10
The Jackson Laboratory