|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form of cataract in which the lens substance has shrunk, leaving a collapsed, flattened capsule with little or no cortex or epithelium on the lens. (Human Phenotype Ontology, HP_0010922)|
|Downloads & Tools|
1 genes associated with the membranous cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|CRYGS||crystallin, gamma S|