All individuals with variants in gene KERA

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

ID_report     

Reference     

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Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

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Owner     
00331854 11DG0866 PubMed: Alsaif 2019 familial - - Saudi Arabia - - - - - retinal disease primary congenital glaucoma, severe anterior segment dysgenesis (prior surgeries may have been a confounding factor) 1 1 LOVD
00434207 Fam17PatI PubMed: Jackson 2020 family M - Pakistan Asia - - - - ? anterior segment dysgenesis; sclerocornea; microcornea; microphthalmos, high hypermetropia 1 2 Johan den Dunnen
00434209 Fam21PatI PubMed: Jackson 2020 family F - Pakistan Asia - - - - ? cornea plana; high hypermetropia; central opacification of the cornea; amblyopia 1 2 Johan den Dunnen
00434223 Fam17PatII PubMed: Jackson 2020 sib M - Pakistan Asia - - - - ? anterior segment dysgenesis; microcornea; microphthalmos, high hypermetropia; exotropia; conical tooth 1 1 Johan den Dunnen
00434224 Fam21PatII PubMed: Jackson 2020 sib M - Pakistan Asia - - - - ? cornea plana; high hypermetropia; central opacification of the cornea; amblyopia 1 1 Johan den Dunnen
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