Phenotypes for disease #04445 (CMT2T (Charcot-Marie-Tooth disease,? axonal, type 2T (CMT-2T)), OMIM:616233)

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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     
0000321077 - - - Familial, autosomal dominant 66 - 50y? walking difficulties - Marco Savarese 00430268
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