Charcot-Marie-Tooth disease X-linked recessive 4

Summary

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: axonal motor sensory neuropathy with deafness and mental retardation, Charcot-Marie-Tooth disease with deafness and mental retardation, CMT4X, CMTX4, Cowchock syndrome, COWCK, NADMR, X-linked Charcot-Marie-Tooth disease type 4, NAMSD

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, 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), X-linked recessive disease (is_a)