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Disease Ontology Browser
Charcot-Marie-Tooth disease axonal type 2L (DOID:0110174)
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2L; autosomal dominant Charcot-Marie-Tooth disease type 2L; Charcot-Marie-Tooth neuropathy axonal type 2L; CMT2L
Alt IDs: OMIM:608673, ICD10CM:G60.0, ORDO:99945
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 gene.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory