About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 76 (DOID:0110821)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 76; SPG76
Alt IDs: OMIM:616907
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.

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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.20
The Jackson Laboratory