partial central choroid dystrophy 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_9822)
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19 genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRPH2 peripherin 2 (retinal degeneration, slow) 1.9094
GUCA1A guanylate cyclase activator 1A (retina) 1.71727
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 1.69315
PITPNA phosphatidylinositol transfer protein, alpha 1.58091
UNC119 unc-119 homolog (C. elegans) 1.31275
RIMS1 regulating synaptic membrane exocytosis 1 1.26124
TIMP3 TIMP metallopeptidase inhibitor 3 1.14857
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1.03493
RING1 ring finger protein 1 1.03409
AIPL1 aryl hydrocarbon receptor interacting protein-like 1 0.992752
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1 0.941611
ERG v-ets avian erythroblastosis virus E26 oncogene homolog 0.933727
ARRB2 arrestin, beta 2 0.879424
RCVRN recoverin 0.843802
PLIN2 perilipin 2 0.774932
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) 0.774932
NPR1 natriuretic peptide receptor 1 0.482844
GUCY2C guanylate cyclase 2C 0.482084
PROM1 prominin 1 0.305587