| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010922 |
| Similar Terms | |
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1 genes associated with the membranous cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CRYGS | crystallin, gamma S |
