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cataract 18

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Any cataract in which the cause of the disease is a mutation in the FYCO1 gene.
Uniprot Description An opacification of the crystalline lens of the eye becoming evident at birth or in infancy. It frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function.
Mondo Term and Equivalent IDs
MONDO:0012395:  cataract 18
DOID:0110238: cataract 18
GARD:0009892: 
MESH:C535337: