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DOID:0110200 - Charcot-Marie-Tooth disease dominant intermediate D
Disease Ontology Definition:A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23.
Synonyms: CMTDID, Charcot-Marie-Tooth neuropathy dominant intermediate D, DI-CMTD, autosomal dominant intermediate Charcot-Marie-Tooth disease type D,
Echinobase Genes :
MIM:607791 - charcot-marie-tooth disease, dominant intermediate d; cmtdid |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee