Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110181 - Charcot-Marie-Tooth disease axonal type 2Z

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MORC2 gene on chromosome 22q12.

Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z, Charcot-Marie-Tooth neuropathy type 2Z, CMT2Z

Xenbase Genes : morc2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014736 - Charcot-Marie-Tooth disease axonal type 2Z

MIM:
MIM:616688 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z

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)