autosomal recessive sensory neuropathy with spastic paraplegia 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

autosomal recessive sensory neuropathy with spastic paraplegia (DOID:0061188)
Alliance: disease page
Alt IDs: OMIM:256840
Definition: A hereditary sensory neuropathy that has_material_basis_in homozygous mutation in the CCT5 gene.

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 08/05/2025 MGI 6.24