Phenotypes for disease #02587 (CMTDIB;CMT2M (Charcot-Marie-Tooth disease, dominant intermediate, type B (CMTDIB, axonal, type 2M (CMT-2M))), OMIM:606482)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000291859 Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762) CMT - Unknown 67y - - - - Yvet den Hartog 00398775
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