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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,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Charcot-Marie-Tooth disease type 2 (is_a)