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Disease Ontology Browser
hereditary spastic paraplegia 24 (DOID:0110775)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 24; autosomal recessive spastic paraplegia type 24; SPG24
Alt IDs: OMIM:607584, ICD10CM:G11.4, ORDO:101004
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 13q14.

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
MGI 6.20
The Jackson Laboratory