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Disease Ontology Browser
hereditary spastic paraplegia 41 (DOID:0110793)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 41; autosomal dominant spastic paraplegia type 41; SPG41
Alt IDs: OMIM:613364, ICD10CM:G11.4, ORDO:320355
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.


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
02/18/2020
MGI 6.14
The Jackson Laboratory