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Disease Ontology Browser
hereditary spastic paraplegia 73 (DOID:0110818)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 73; autosomal dominant spastic paraplegia type 73; SPG73
Alt IDs: OMIM:616282, ICD10CM:G11.4, ORDO:444099
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13.


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
09/27/2022
MGI 6.21
The Jackson Laboratory