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Disease Ontology Browser
hereditary spastic paraplegia 55 (DOID:0110807)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 55; autosomal recessive spastic paraplegia type 55; SPG55
Alt IDs: OMIM:615035, ICD10CM:G11.4, ORDO:320375
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24.


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
11/10/2020
MGI 6.16
The Jackson Laboratory