Phenotypes for disease #00402 (OCCO (coloboma, ocular (OCCO)))

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000333619 see paper; ..., no microphthalmia; R iris, choroidal, and optic disc coloboma; L choroidal and optic disc coloboma; right cortical cataract; bilateral congenital deafness; neurocognitive difficulties coloboma - Unknown 10y - - - - Johan den Dunnen 00444366
0000333620 see paper; ..., no microphthalmia; R optic disc coloboma; L iris and optic disc coloboma with cortical cataract; congenital nystagmus, high myopia coloboma - Unknown 43y - - - - Johan den Dunnen 00444367
0000333621 see paper; ..., no microphthalmia; bilateral iris and large chorioretinal coloboma, with R posterior cataract; secondary congenital nystagmus, high myopia coloboma - Familial, autosomal dominant 26y - - - - Johan den Dunnen 00444368
0000333622 see paper; ..., bilateral OD coloboma coloboma - Unknown - - - - - Johan den Dunnen 00444369
0000333623 see paper; ..., no microphthalmia; bilateral iris coloboma, with unilateral hyperopia; diaphragmatic hernia coloboma - Unknown 6y - - - - Johan den Dunnen 00444370
0000333624 see paper; ..., no microphthalmia; R iris coloboma; L macular and optic disc coloboma coloboma - Unknown 15y - - - - Johan den Dunnen 00444371
0000333625 see paper; ..., no microphthalmia; bilateral retinal coloboma coloboma - Unknown 75y - - - - Johan den Dunnen 00444372
0000333626 see paper; ..., microphthalmia, intellectual disability, autistic features, craniofacial dysmorphy with scaphocephaly, no rhizomelic skeletal dysplasia; father isolated bilateral colobomatous microphthalmia coloboma - Familial, autosomal dominant 30y - - - - Johan den Dunnen 00444373
0000333627 see paper; ..., microphthalmia; bilateral optic disc coloboma with unilateral microphthalmia coloboma - Familial, autosomal dominant 7y - - - - Johan den Dunnen 00444374
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