Phenotypes for disease #03781 (CMT4F (Charcot-Marie-Tooth disease, type 4F (CMT-4F)), OMIM:614895)

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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     
0000357070 Scoliosis Congenital myopathy CMT4F Familial, autosomal recessive - - - - - Camille Verebi 00472261
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