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Disease Ontology Browser
Charcot-Marie-Tooth disease type 2B (DOID:0110159)
Synonyms: autosomal dominant Charcot-Marie-Tooth disease type 2B; Charcot-Marie-Tooth neuropathy type 2B; CMT2B; hereditary motor and sensory nueropathy IIB; HMSN2B; HMSN IIB
Alt IDs: OMIM:600882, ICD10CM:G60.0, ORDO:99936
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the RAB7 gene on chromosome 3q21.


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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
06/20/2017
MGI 6.10
The Jackson Laboratory