hereditary spastic paraplegia 73 Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24