Phenotypes for disease #02356 (CMT4B1 (Charcot-Marie-Tooth disease, type 4B1 (CMT-4B1)), OMIM:601382)

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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     
0000291835 Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) CMT CMT4B1 Familial, autosomal recessive 30y - 22y Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) - Yvet den Hartog 00398752
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