Pseudopapilledema Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1392)
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Genes

42 genes co-occuring with the disease Pseudopapilledema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
FAM111A family with sequence similarity 111, member A 2.09
MFRP membrane frizzled-related protein 2.002
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis) 1.974
AIPL1 aryl hydrocarbon receptor interacting protein-like 1 1.918
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 1.833
PRSS56 protease, serine, 56 1.731
RD3 retinal degeneration 3 1.653
ADAMTSL4 ADAMTS-like 4 1.603
CEP290 centrosomal protein 290kDa 1.588
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1 1.582
RPE65 retinal pigment epithelium-specific protein 65kDa 1.577
TBCE tubulin folding cofactor E 1.539
CRX cone-rod homeobox 1.516
CLUL1 clusterin-like 1 (retinal) 1.431
RAX retina and anterior neural fold homeobox 1.386
TRIM31 tripartite motif containing 31 1.289
CYLC1 cylicin, basic protein of sperm head cytoskeleton 1 1.265
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1.252
NLRP3 NLR family, pyrin domain containing 3 1.247
ZNF587 zinc finger protein 587 1.235
FBN2 fibrillin 2 1.229
SMAD4 SMAD family member 4 1.222
CLSTN3 calsyntenin 3 1.182
ATPSCKMT ATP synthase c subunit lysine N-methyltransferase 1.182
ERCC6 excision repair cross-complementation group 6 1.18
CA5B carbonic anhydrase VB, mitochondrial 1.166
MOG myelin oligodendrocyte glycoprotein 1.156
DPYSL5 dihydropyrimidinase-like 5 1.14
MINPP1 multiple inositol-polyphosphate phosphatase 1 1.133
SLC25A6 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6 1.126
MISP mitotic spindle positioning 1.124
NR2E3 nuclear receptor subfamily 2, group E, member 3 1.121
RDH8 retinol dehydrogenase 8 (all-trans) 1.09
LRRC3 leucine rich repeat containing 3 1.087
CA5A carbonic anhydrase VA, mitochondrial 1.083
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1 1.045
OPTC opticin 1.043
SPATA7 spermatogenesis associated 7 1.031
LCA5 Leber congenital amaurosis 5 1.021
PGLYRP2 peptidoglycan recognition protein 2 1.021
BMPR1A bone morphogenetic protein receptor, type IA 1.018
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class) 1.012