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Disease Ontology Browser
hereditary spastic paraplegia 11 (DOID:0110764)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 11; autosomal recessive spastic paraplegia complicated with thin corpus callosum; autosomal recessive spastic paraplegia type 11; autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum; HSP-TCC; Nakamura-Osame syndrome; spastic paraplegia-intellectual disability-thin corpus callosum syndrome; SPG11
Alt IDs: OMIM:604360, ICD10CM:G11.4, ORDO:2822
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.

Disease References using Mouse Models (1)

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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MGI 6.17
The Jackson Laboratory