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Charcot-Marie-Tooth disease type 2B (DOID:0110159)
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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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