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DOID:0110175 - Charcot-Marie-Tooth disease axonal type 2O
Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32.
Synonyms: Charcot-Marie-Tooth neuropathy axonal type 2O, autosomal dominant Charcot-Marie-Tooth disease type 2O, autosomal dominant axonal Charcot-Marie-Tooth disease type 2O,
Xenbase Genes : dync1h1
MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee