Summary Literature (0)

DOID:0110162 - Charcot-Marie-Tooth disease, axonal type 2W

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31.

Synonyms: CMT2W, Charcot-Marie-Tooth neuropathy type 2W, autosomal dominant axonal Charcot-Marie-Tooth disease type 2W,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014711 - autosomal dominant Charcot-Marie-Tooth disease type 2W

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee