Charcot-Marie-Tooth disease, axonal type 2W

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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

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

Parent(s): autosomal dominant disease (is_a), Charcot-Marie-Tooth disease type 2 (is_a)