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DOID:0110212 - Charcot-Marie-Tooth disease X-linked recessive 4
Disease Ontology Definition:A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26.
Synonyms: CMT4X, CMTX4, COWCK, Charcot-Marie-Tooth disease with deafness and mental retardation, Cowchock syndrome, NADMR, NAMSD, X-linked Charcot-Marie-Tooth disease type 4, axonal motor sensory neuropathy with deafness and mental retardation,
Echinobase Genes
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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 X (is_a)