About   Help   FAQ
Disease Ontology Browser
Charcot-Marie-Tooth disease type 2B (DOID:0110159)
Alliance: disease page
Synonyms: autosomal dominant Charcot-Marie-Tooth disease type 2B; Charcot-Marie-Tooth neuropathy type 2B; CMT2B; hereditary motor and sensory nueropathy IIB; HMSN2B; HMSN IIB
Alt IDs: OMIM:600882, ICD10CM:G60.0, MESH:C537989, ORDO:99936
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the RAB7 gene on chromosome 3q21.

Disease References using Mouse Models (1)
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