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Echinobase
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:
OMIM: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
Parent(s): Charcot-Marie-Tooth disease type 2 (is_a)