About   Help   FAQ
Disease Ontology Browser
Charcot-Marie-Tooth disease type 2B2 (DOID:0110179)
Alliance: disease page
Synonyms: AR-CMT2B2; ARCMT2B; autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2; Autosomal recessive axonal CMT4C3; Charcot-Marie-Tooth disease neuronal type 2B2; Charcot-Marie-Tooth neuropathy type 2B2; CMT2B2
Alt IDs: OMIM:605589, ICD10CM:G60.0, ORDO:101101
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the MED25 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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory