About   Help   FAQ
Disease Ontology Browser
Charcot-Marie-Tooth disease axonal type 2L (DOID:0110174)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2L; autosomal dominant Charcot-Marie-Tooth disease type 2L; Charcot-Marie-Tooth neuropathy axonal type 2L; CMT2L
Alt IDs: OMIM:608673, ICD10CM:G60.0, ORDO:99945
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 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
12/10/2024
MGI 6.24 		The Jackson Laboratory