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Disease Ontology Browser
Charcot-Marie-Tooth disease axonal type 2V (DOID:0110178)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2V; autosomal dominant Charcot-Marie-Tooth disease type 2V; Charcot-Marie-Tooth neuropathy type 2V; CMT2V
Alt IDs: OMIM:616491, ORDO:447964
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.


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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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last database update
07/02/2024
MGI 6.13
The Jackson Laboratory