retinal drusen Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2569)
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10 genes co-occuring with the disease retinal drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
IMPG1 interphotoreceptor matrix proteoglycan 1 1.54054
CFH complement factor H 1.42191
BAK1 BCL2-antagonist/killer 1 1.05681
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1 1.02735
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6 0.830689
CFB complement factor B 0.765535
COL4A5 collagen, type IV, alpha 5 0.754934
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 0.741923
CD44 CD44 molecule (Indian blood group) 0.243995
CD68 CD68 molecule 0.223509