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DOID:0110173 - Charcot-Marie-Tooth disease axonal type 2U
Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MARS gene on chromosome 12q13.
Synonyms: CMT2U, Charcot-Marie-Tooth neuropathy type 2U, autosomal dominant Charcot-Marie-Tooth disease type 2U, autosomal dominant axonal Charcot-Marie-Tooth disease type 2U,
Echinobase Genes

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)