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Disease Ontology Browser
Charcot-Marie-Tooth disease, axonal type 2W (DOID:0110162)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2W; Charcot-Marie-Tooth neuropathy type 2W; CMT2W
Alt IDs: OMIM:616625
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31.

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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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11/12/2024
MGI 6.24 		The Jackson Laboratory