Summary Literature (0)

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,

Echinobase Genes : dync1h1


OMIM:

MIM:614228 - charcot-marie-tooth disease, axonal, type 2o; cmt2o

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

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