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Disease Ontology Browser
Charcot-Marie-Tooth disease type 4G (DOID:0110196)
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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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MGI 6.20
The Jackson Laboratory