About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 32 (DOID:0110783)
Alliance: disease page
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory