Phenotypes for disease #03841 (PEOA6 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 6 (PEOA-6)), OMIM:615156)

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     
0000326573 Elevated circulating creatine kinase concentration, Myalgia, Triggered by febrile illness - - Unknown 06y - - - - Andreas Laner 00436392
0000326575 External ophthalmoplegia, Facial muscle weakness, mtDNA deletions seen on muscle biopsy - - Unknown 86y - - - - Andreas Laner 00436395
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