Phenotypes for disease #05209 (ODA (Ocular developmental anomalies))

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000069602 Microphthalmia, cataract, sclerocornea - - Unknown - - - - - Michel van Geel 00090264
0000069677 colobomatous microphthalmia, corpus callosum abnormality and atrial septel defects. - - Familial, autosomal dominant - - - - - Michel van Geel 00090967
0000069678 colobomatous microphthalmia, corpus callosum abnormality and atrial septel defects. - - Familial, autosomal dominant - - - - - Michel van Geel 00090968
0000069743 bilateral Axenfeld-Rieger malformation - - Familial, autosomal dominant - - - - - Michel van Geel 00091296
0000069744 bilateral Peters anomaly - - Familial, autosomal dominant - - - - - Michel van Geel 00091297
0000069745 autosomal dominant AM-ASD - - Familial, autosomal dominant - - - - - Michel van Geel 00091298
0000069746 bilateral Peters anomaly - - Familial, autosomal dominant - - - - - Michel van Geel 00091299
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