Phenotypes for disease #02541 (NEM5 (myopathy, nemaline, type 5 (NEM-5)), OMIM:605355)

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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     
0000357033 Muscle weakness, Generalized limb muscle atrophy Congenital myopathy NEM5C Isolated (sporadic) - - - - - Camille Verebi 00472224
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