About   Help   FAQ
Disease Ontology Browser
Charcot-Marie-Tooth disease axonal type 2H (DOID:0110166)
Alliance: disease page
Synonyms: AR-CMT2C; autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features; autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features; Autosomal recessive axonal CMT4C2; Axonal Charcot-Marie-Tooth disease with pyramidal involvement; Charcot-Marie-Tooth disease type 2H; CMT2H
Alt IDs: OMIM:607731, ICD10CM:G60.0, ORDO:101102
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in variation in the region 8q13-q23.

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