Phenotypes for disease #02026 (CEP (porphyria, erythropoietic, congenital (CEP)), OMIM:263700)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000105565 see paper; ... - - Familial, autosomal recessive 15y - 00y00m01d photosensitivity, hepatosplenomegaly, anemia - Johan den Dunnen 00132802
0000105566 see paper; required red cell transfusions , significant periods during adolescence without treatment, marked cutaneous involvement resulting from unprotected sunlight exposure - - Familial, autosomal recessive 20y - - - - Johan den Dunnen 00132803
0000105567 see paper; chronic, progressive skin ulcerations since adolescence eventually disfigured sun-exposed face/hands; moderately anemic, hemoglobins ranging from 10 to 12 g/dL next decade;56y-hemoglobin 8 g/dL, red cell transfusions administered every 3w - - Familial, autosomal recessive 44y 20y-30y - - - Johan den Dunnen 00132804
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