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DOID:0110168 - Charcot-Marie-Tooth disease type 2Y
Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13.
Synonyms: CMT2 due to VCP mutation, CMT2Y, Charcot-Marie-Tooth neuropathy type 2Y, autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation, autosomal dominant axonal Charcot-Marie-Tooth type 2Y,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014735 - Charcot-Marie-Tooth disease type 2Y |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee