Phenotypes for disease #04245 (PEOA (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant (PEOA)))

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000034300 see paper; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00046789
0000034301 see paper; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00046790
0000034302 see paper; ..., progressive external ophtalmoparesis, cerebellar signs multiple RC complex defect - Familial, autosomal recessive - - 45y - - Johan den Dunnen 00046791
0000281591 bilateral ptosis (HP:0001488), horizontal ophthalmoplegia (HP:0000602), slight bilateral sensory-neuronal hearing impairment (HP:0008619), atrophy of the mesencephalon pedunculus cerebelli superior (HP:0001272), frontotemporal parts of the brain (HP:0006892) - Progressive external ophthalmoplegia (HP:0000544) Familial, autosomal recessive 69y 69y - - - Giovanna Aschettino 00387997
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