Phenotypes for disease #00935 (Birk-Barel mental retardation dysmorphism syndrome, OMIM:612292)

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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     
0000357063 0001290: Generalised hypotonia, 0001270: Motor delay, 0003701: Proximal muscle weakness Congenital myopathy Birk-Barel syndrome Isolated (sporadic) - - - - - Camille Verebi 00472254
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