About   Help   FAQ
Disease Ontology Browser
Charcot-Marie-Tooth disease type 1C (DOID:0110151)
Alliance: disease page
Synonyms: Charcot-Marie-Tooth neuropathy type 1C; CMT1C; CMT slow nerve conduction type C; HMSN1C; HMSN IC; neuropathy hereditary motor and sensory type 1C
Alt IDs: OMIM:601098, ICD10CM:G60.0, MESH:C537984, ORDO:101083
Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.

Disease References using Mouse Models (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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory