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Disease Ontology Browser
Charcot-Marie-Tooth disease type 4A (DOID:0110185)
Alliance: disease page
Synonyms: autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A; Charcot-Marie-Tooth neuropathy type 4A; CMT4A
Alt IDs: OMIM:214400, ICD10CM:G60.0, MESH:C535419, ORDO:99948
Definition: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding ganglioside-induced differentiation-associated protein-1 (GDAP1) on chromosome 8q21.


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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
04/16/2024
MGI 6.23
The Jackson Laboratory