Phenotypes for disease #04497 (PGBM2 (myopathy, polyglucosan body, type 2 (PGBM-2)), OMIM:616199)

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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     
0000357062 0003198: Myopathy, 0003376: Steppage gait, 0003391: Gowers' sign Myopathy PGBM2 Familial, autosomal recessive - - - - - Camille Verebi 00472253
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