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Charcot-Marie-Tooth disease type 2Y (DOID:0110168)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth type 2Y; autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation; Charcot-Marie-Tooth neuropathy type 2Y; CMT2 due to VCP mutation; CMT2Y
Alt IDs: OMIM:616687, ICD10CM:G60.0, ORDO:435387
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13.

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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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12/10/2024
MGI 6.24 		The Jackson Laboratory