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DOID:0110160 - Charcot-Marie-Tooth disease axonal type 2T
Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.
Synonyms: autosomal recessive axonal Charcot-Marie-Tooth disease type 2T, Charcot-Marie-Tooth neuropathy type 2T, CMT2T, AR-CMT2T
Echinobase Genes
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Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
autosomal recessive disease (is_a),
Charcot-Marie-Tooth disease type 2 (is_a)