Phenotypes for disease #01455

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000042989 centronuclear myopathy, neonatal-onset - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056376
0000042990 centronuclear myopathy with cataracts - - Unknown - - - - - Johan den Dunnen 00056377
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