Phenotypes for disease #05147 (CPEO (ophthalmoplegia, external, progressive, chronic (CPEO)))

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000046777 CPEO - - Unknown - - - - - Andreas Laner 00037297
0000046778 CPEO - - Unknown - - - - - Andreas Laner 00037299
0000155153 - - - Familial, autosomal recessive 52y 48y 45y - - André Militão 00207382
0000249496 - - - Familial, autosomal recessive - - - - - Le Guo 00331302
0000281503 strabismus (HP:0000486), ophthalmoplegia (HP:0000602), bilateral ptosis (HP:0001488), exotropia ( HP:0000577), ophthalmoparesis ( HP:0000597), Abnormality of eye movement ( HP:0000496) - progressive external ophthalmoplegia (HP:0000590) Familial, autosomal recessive 33y 33y - - - Giovanna Aschettino 00384650
0000333191 ptosis (HP:0000508), Respiratory insufficiency due to muscle weakness (HP:0002747); Global developmental delay(HP:0001263); Hypotonia (HP:0001252) ;Weakness of facial musculature(HP:0030319); Ophthalmoparesis (HP:0000597); High palate (HP:0000218 congenital myasthenia Pure mitochondrial myopathy Familial, autosomal recessive 05y - 01y06m Fatigable weakness of bulbar muscles(HP:0030192) SURF1 Beatriz Betini 00443912
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