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DOID:0110158 - Charcot-Marie-Tooth disease type 2I
Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23.
Synonyms: CMT2I, Charcot-Marie-Tooth neuropathy type 2I,
Echinobase Genes

OMIM:607677 - charcot-marie-tooth disease, axonal, type 2i; cmt2i |
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)