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Charcot-Marie-Tooth disease X-linked recessive 4 (DOID:0110212)
Alliance: disease page
Synonyms: axonal motor sensory neuropathy with deafness and mental retardation; Charcot-Marie-Tooth disease with deafness and mental retardation; CMT4X; CMTX4; Cowchock syndrome; NADMR; NAMSD; X-linked Charcot-Marie-Tooth disease type 4
Alt IDs: OMIM:310490, ICD10CM:G60.0, ORDO:101078
Definition: A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory