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Disease Ontology Browser
Charcot-Marie-Tooth disease type 4G (DOID:0110196)
Alliance: disease page
Synonyms: autosomal recessive Charcot-Marie-Tooth disease type 4G; Charcot-Marie-Tooth neuropathy type 4G; CMT4G; hereditary motor and sensory neuropathy Russe type; HMSNR
Alt IDs: OMIM:605285, ICD10CM:G60.0, ORDO:99953
Definition: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.


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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
02/13/2024
MGI 6.23
The Jackson Laboratory