Phenotypes for disease #04337 (FECD (dystrophy, corneal, Fuchs endothelial (FECD)))

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000127802 see paper; ..., fully penetrant dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155303
0000127803 - dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155304
0000127804 see paper; … dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155305
0000127805 see paper; … dystrophy, corneal, Fuchs endothelial (FECD) - Familial, autosomal dominant - - - - - Johan den Dunnen 00155306
0000127806 see paper; … dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155307
0000127807 see paper; … dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155308
0000127808 see paper; … dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155309
0000127809 see paper; ... dystrophy, corneal, Fuchs endothelial FECD-3 Familial, autosomal dominant - - - - - Johan den Dunnen 00155310
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