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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)
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last database update
02/13/2024
MGI 6.23
The Jackson Laboratory