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cataract 20 multiple types
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any cataract (disease) in which the cause of the disease is a mutation in the CRYGS gene.
Uniprot Description An opacification of the crystalline lens of the eye that 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. CTRCT20 includes progressive polymorphic anterior, posterior, or peripheral cortical.
Disease Ontology Description A cataract that has_material_basis_in heterozygous mutation in the CRYGS gene on chromosome 3q27.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110240
OMIM:116100
MONDO:0007284
High level summary of knowledge for a disease, including descriptions and datasource references.