Congenital Retinal Fold

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Results for "Congenital Retinal Fold": 1001 gene sets

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Congenital Retinal Fold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Retinal Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
falciform retinal fold Gene Set From HPO Gene-Disease Associations genes associated with the falciform retinal fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Retinal Fold (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Fold (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
Retinal detachment or retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment or retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal detachment with retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment with retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypertrophy of retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypertrophy of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal nonattachment, nonsyndromic congenital Gene Set From OMIM Gene-Disease Associations genes associated with the retinal nonattachment, nonsyndromic congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Hypertrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypertrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment, Nonsyndromic Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Amaurosis Of Retinal Origin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Amaurosis Of Retinal Origin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Retinal Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Retinal Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
fold Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term fold in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
morphogenesis of an epithelial fold Gene Set From GO Biological Process Annotations 2015 genes participating in the morphogenesis of an epithelial fold biological process from the curated GO Biological Process Annotations 2015 dataset.
neural fold formation Gene Set From GO Biological Process Annotations 2015 genes participating in the neural fold formation biological process from the curated GO Biological Process Annotations 2015 dataset.
neural fold bending Gene Set From GO Biological Process Annotations 2015 genes participating in the neural fold bending biological process from the curated GO Biological Process Annotations 2015 dataset.
neural fold elevation formation Gene Set From GO Biological Process Annotations 2015 genes participating in the neural fold elevation formation biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormality of the aryepiglottic fold Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prominent nasolabial fold Gene Set From HPO Gene-Disease Associations genes associated with the prominent nasolabial fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thickened nuchal skin fold Gene Set From HPO Gene-Disease Associations genes associated with the thickened nuchal skin fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Kringle-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kringle-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
UBA/THIF-type NAD/FAD binding fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the UBA/THIF-type NAD/FAD binding fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ubiquitin-fold modifier 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-fold modifier 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rossmann-like alpha/beta/alpha sandwich fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rossmann-like alpha/beta/alpha sandwich fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Carbohydrate-binding-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbohydrate-binding-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Histone-fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane-anchored ubiquitin-fold protein, HCG-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-anchored ubiquitin-fold protein, HCG-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Staphylococcal nuclease (SNase-like), OB-fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Staphylococcal nuclease (SNase-like), OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein L30, ferredoxin-like fold domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L30, ferredoxin-like fold domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nucleolar GTP-binding protein 1, Rossman-fold domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleolar GTP-binding protein 1, Rossman-fold domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-grasp fold, subdomain 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-grasp fold, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-grasp fold, subdomain 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-grasp fold, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thioredoxin-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thioredoxin-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha/Beta hydrolase fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha/Beta hydrolase fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha/beta hydrolase fold-3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha/beta hydrolase fold-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha/beta hydrolase fold-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha/beta hydrolase fold-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha/beta hydrolase fold-5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha/beta hydrolase fold-5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Immunoglobulin-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Phenylalanine-tRNA ligase, beta subunit, ferrodoxin-fold anticodon-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Phenylalanine-tRNA ligase, beta subunit, ferrodoxin-fold anticodon-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pectin lyase fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pectin lyase fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BTB/POZ fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BTB/POZ fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rad4/PNGase transglutaminase-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rad4/PNGase transglutaminase-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peptidase C78, ubiquitin fold modifier-specific peptidase 1/ 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase C78, ubiquitin fold modifier-specific peptidase 1/ 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-grasp fold, succinyl-CoA synthetase-type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-grasp fold, succinyl-CoA synthetase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ubiquitin-fold modifier-conjugating enzyme 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-fold modifier-conjugating enzyme 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PAS fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PAS fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pectin lyase fold/virulence factor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pectin lyase fold/virulence factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Flavodoxin-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Flavodoxin-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-grasp fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-grasp fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein S5 domain 2-type fold, subgroup Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S5 domain 2-type fold, subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nucleic acid-binding, OB-fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleic acid-binding, OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
OB-fold nucleic acid binding domain, AA-tRNA synthetase-type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the OB-fold nucleic acid binding domain, AA-tRNA synthetase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PAS fold-3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PAS fold-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RmlC-like jelly roll fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RmlC-like jelly roll fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-grasp fold, RimK-type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-grasp fold, RimK-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RNA polymerase Rpb2, OB-fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA polymerase Rpb2, OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rubredoxin-type fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rubredoxin-type fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tissue inhibitor of metalloproteinases-like, OB-fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tissue inhibitor of metalloproteinases-like, OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
C-type lectin fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the C-type lectin fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
LamG-like jellyroll fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the LamG-like jellyroll fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamin diphosphate-binding fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamin diphosphate-binding fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein S5 domain 2-type fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S5 domain 2-type fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Armadillo-type fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Armadillo-type fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Plexin-like fold Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Plexin-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Clathrin, heavy chain/VPS, 7-fold repeat Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Clathrin, heavy chain/VPS, 7-fold repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal neural fold elevation formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cephalic neural fold morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cephalic neural fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of head fold formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of head fold formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal head fold morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal head fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neural fold formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal urogenital fold morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal urogenital fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neural fold morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vocal fold Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue vocal fold in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Skin Fold (Abnormality) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Skin Fold (Abnormality) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Descemet'S Membrane Fold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Descemet'S Membrane Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Aryepiglottic Fold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Aryepiglottic Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thickened Nuchal Skin Fold Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thickened Nuchal Skin Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prominent Nasolabial Fold Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prominent Nasolabial Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Underdeveloped Nasolabial Fold Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Underdeveloped Nasolabial Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infra-Orbital Fold Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infra-Orbital Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neural fold bending Gene Set From GO Biological Process Annotations 2023 genes participating in the neural fold bending biological process from the curated GO Biological Process Annotations 2023 dataset.
morphogenesis of an epithelial fold Gene Set From GO Biological Process Annotations 2023 genes participating in the morphogenesis of an epithelial fold biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal head fold morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal head fold morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neural fold formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neural fold formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina fold Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fold phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cephalic neural fold morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cephalic neural fold morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neural fold elevation formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent head fold Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent head fold phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neural fold morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neural fold morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal urogenital fold morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urogenital fold morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Vocal fold Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vocal fold in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Subscapular skin fold thickness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subscapular skin fold thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhegmatogenous retinal detachment, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal degeneration, autosomal recessive, clumped pigment type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
retinal dimer Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical retinal dimer from the curated CTD Gene-Chemical Interactions dataset.
9-cis-retinal Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.
13-cis-retinal Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 13-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.
Retinal Cone Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
Retinal Detachment Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Detachment from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, retinal, 1, North Carolina type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.
Retinal Artery Occlusion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Artery Occlusion from the curated CTD Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy from the curated CTD Gene-Disease Associations dataset.
Macular Dystrophy, Retinal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.
Retinal Dystrophies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Dystrophies from the curated CTD Gene-Disease Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.
Retinal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Diseases from the curated CTD Gene-Disease Associations dataset.
MACULAR DYSTROPHY, RETINAL, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Retinal Vein Occlusion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Vein Occlusion from the curated CTD Gene-Disease Associations dataset.
Doyne honeycomb retinal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.
RETINAL DYSPLASIA, PRIMARY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.
Retinal cone dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Retinal Telangiectasis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Telangiectasis from the curated CTD Gene-Disease Associations dataset.
Retinal Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Retinal Vein Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Retinal Vein in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
retinal cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal cell cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal cell cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal vascular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal microaneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal microaneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vascular occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vascular occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
abnormal retinal correspondence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal perforation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acute retinal necrosis syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute retinal necrosis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vascular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
branch retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease branch retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal hemangioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal hemangioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal detachment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal detachment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetes complications; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
branch retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease branch retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal function Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing loss/deafness; retinal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; retinal vascular occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal detachment; vitreoretinopathy, proliferative Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal detachment; vitreoretinopathy, proliferative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vascular occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal detachment Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal detachment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
night blindness; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease night blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; retinal vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
color vision defects; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet's disease; retinal vasculitis; uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet's disease; retinal vasculitis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal neoplasms; retinoblastoma Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal neoplasms; retinoblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vascular occlusive disease Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vascular occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neovascularization, pathologic; retinal vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease neovascularization, pathologic; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; inflammation; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; inflammation; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal dystrophies; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal dystrophies; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term retinal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal bipolar neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal isomerase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
all-trans-retinal Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the all-trans-retinal ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Retinal vascular caliber Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Rhegmatogenous retinal detachment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
retinal degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal detachment Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal detachment in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal vascular disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal vascular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of retinal arteries Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
retinal coloboma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the retinal coloboma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
rhegmatogenous retinal detachment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
retinal detachment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the retinal vasculature Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
4-OH-Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the 4-OH-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
9-cis-Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the 9-cis-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
retinal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal striation Gene Set From HPO Gene-Disease Associations genes associated with the retinal striation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacunar retinal depigmentation Gene Set From HPO Gene-Disease Associations genes associated with the lacunar retinal depigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal retinal infarction Gene Set From HPO Gene-Disease Associations genes associated with the focal retinal infarction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
exudative retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the exudative retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tractional retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the tractional retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macroreticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macroreticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rarefaction of retinal pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the rarefaction of retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal retinal folds Gene Set From HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large hyperpigmented retinal spots Gene Set From HPO Gene-Disease Associations genes associated with the large hyperpigmented retinal spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal telangiectasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal telangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal pigmentation abnormalities Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal pigmentation abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the absent retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
depigmented lesions of the retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the depigmented lesions of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
achromatic retinal patches Gene Set From HPO Gene-Disease Associations genes associated with the achromatic retinal patches phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal calcification Gene Set From HPO Gene-Disease Associations genes associated with the retinal calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular malformation Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the retinal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal flecks Gene Set From HPO Gene-Disease Associations genes associated with the retinal flecks phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar constriction Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar constriction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal avascularization Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal avascularization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal pigment epithelial atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal nonattachment Gene Set From HPO Gene-Disease Associations genes associated with the retinal nonattachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased retinal pigmentation with dispersion Gene Set From HPO Gene-Disease Associations genes associated with the decreased retinal pigmentation with dispersion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal malformation Gene Set From HPO Gene-Disease Associations genes associated with the retinal malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the retinal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal deposits Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the retinal vasculature Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the retinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular retinal pigment epithelial mottling Gene Set From HPO Gene-Disease Associations genes associated with the macular retinal pigment epithelial mottling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal retinal pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar occlusion Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar occlusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the reticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of retinal arteries Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of retinal arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rhegmatogenous retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the rhegmatogenous retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
honeycomb retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the honeycomb retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypermyelinated retinal fibers Gene Set From HPO Gene-Disease Associations genes associated with the hypermyelinated retinal fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal coloboma Gene Set From HPO Gene-Disease Associations genes associated with the retinal coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal exudate Gene Set From HPO Gene-Disease Associations genes associated with the retinal exudate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hamartoma Gene Set From HPO Gene-Disease Associations genes associated with the retinal hamartoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystic retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular proliferation Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular proliferation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
attenuation of retinal blood vessels Gene Set From HPO Gene-Disease Associations genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral traction retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the peripheral traction retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hemangioblastoma Gene Set From HPO Gene-Disease Associations genes associated with the retinal hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Retinal Detachment Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Detachment phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Artery Occlusion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Artery Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Dystrophies Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Dystrophies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Vein Occlusion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Vein Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Drusen Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Drusen phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Vasculitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Vasculitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Neovascularization Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Neovascularization phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Perforations Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Perforations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal pigment epithelium GPCR Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal pigment epithelium GPCR protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal-specific ATP-binding cassette transporter Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal protein C2orf71 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal cGMP phosphodiesterase, gamma subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal cGMP phosphodiesterase, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Visual pigments (opsins) retinal binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal degeneration protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal retinal photoreceptor layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner nuclear layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal melanocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal ganglion cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell inner segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal inner plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal neuronal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal neuronal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer nuclear layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal outer nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal rod cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thick retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thick retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod cell outer segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal layers Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal layers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal photoreceptor morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal blood vessel morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal progenitor cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal deposits Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal induced retinal neovascularization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal ganglion layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ischemia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ischemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal outer nuclear layer degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal rod cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal detachment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal detachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal cone cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal gliosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal gliosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal inner nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal vasculature morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal vasculature morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ganglion cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer plexiform layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal ganglion cell Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal ganglion cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal cone cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal cone cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer nuclear layer thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal spots Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal spots phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal blood vessel pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal inner plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal rod cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced retinal damage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal nerve fiber layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal nerve fiber layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod cell inner segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal photoreceptor degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal photoreceptor degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal outer plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal outer nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal pigment epithelium morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal outer plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner plexiform layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner nuclear layer thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal inner nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal neovascularization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell outer segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal melanin granule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{retinal disease in usher syndrome type iia, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
bothnia retinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, late-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, autosomal recessive, clumped pigment type Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal cone dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3b Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
vasculopathy, retinal, with cerebral leukodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
Biosynthesis of A2E, implicated in retinal degradation Gene Set From Reactome Pathways 2014 proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways dataset.
retinal rod Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal rod from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal pigment epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal cone Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal cone from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal microvascular endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal microvascular endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal ganglion cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal ganglion cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal stem cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal cone Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal rod Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal rod in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal ganglion cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal ganglion cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Neural retinal development(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Neural retinal development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eye-retinal bipolar neuron Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal bipolar neuron relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal blood vessel endothelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal blood vessel endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal ganglion cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal ganglion cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal pigment epithelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal pigment epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Retinal Astrocytic Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Astrocytic Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelial Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelial Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelium Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Toxicity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Toxicity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Venous Retinal Branch Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Venous Retinal Branch Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Necrosis Syndrome, Acute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Necrosis Syndrome, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Retinal Degeneration (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Serous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Serous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Dysplasia And Retinal Aplasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Angiomatous Proliferation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Angiomatous Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Drusen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Retinal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Retinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vasculitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vasculitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Hyperpigmented Retinal Spots Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Large Hyperpigmented Retinal Spots in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Lattice Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Lattice Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Juxtafoveal Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Juxtafoveal Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patterned Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patterned Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmentary Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmentary Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion - Juvenile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion - Juvenile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Microaneurysm With Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Microaneurysm With Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Gliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vascular Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vascular Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Arteriovenous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Microaneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Microaneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Thickening Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thickening in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bothnia Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonperfusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonperfusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Retinal Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Retinal Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Retinal Pigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Retinal Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Attenuation Of Retinal Blood Vessels Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Attenuation Of Retinal Blood Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Flecking Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Flecking in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Mottling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Mottling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Thinning Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Thinning in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peau D'Orange Retinal Changes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peau D'Orange Retinal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Damage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Damage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Depigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Depigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Crystals Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Crystals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choroidal Retinal Neovascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choroidal Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Retinal Vessel Vascular Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Retinal Vessel Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Occlusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Neovascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigmentary Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteries, Tortuosity Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteries, Tortuosity Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypoautofluorescent Retinal Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypoautofluorescent Retinal Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Retinal Avascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Retinal Avascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Exudates Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Exudates in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Achromatic Retinal Patches Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Achromatic Retinal Patches in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arterial Macroaneurysms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arterial Macroaneurysms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Proliferation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Dots Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Dots in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Malformation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Cystoid Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Cystoid Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypermyelinated Retinal Nerve Fibers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermyelinated Retinal Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Tractional Retinal Detachment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Tractional Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
establishment of blood-retinal barrier Gene Set From GO Biological Process Annotations 2023 genes participating in the establishment of blood-retinal barrier biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cone cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cone cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
all-trans retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the all-trans retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
11-cis-retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 11-cis-retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
Retinal Gene Set From MW Enzyme Metabolite Associations interacting proteins for Retinal metabolite from the MW Gene Metabolite Associations dataset.
9-cis-Retinal Gene Set From MW Enzyme Metabolite Associations interacting proteins for 9-cis-Retinal metabolite from the MW Gene Metabolite Associations dataset.
Human - Fetal Development - L1 - Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Retinal ganglion cell_Cerebral organoid_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Cerebral organoid_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Embryonic stem cell_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Embryonic stem cell_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal progenitor cell_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal progenitor cell_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Ganglion cell layer of retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Ganglion cell layer of retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal astrocyte_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal astrocyte_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Neurogenic retinal progenitor cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neurogenic retinal progenitor cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Multipotent retinal progenitor cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Multipotent retinal progenitor cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelium_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelium_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelial cell_Choroid_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelial cell_Choroid_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Eye_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelial cell_Eye_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelial cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Superficial retinal vascular plexus (S-tip cell)_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Superficial retinal vascular plexus (S-tip cell)_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal Müller glia cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal Müller glia cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
GPR143 in melanocytes and retinal pigment epithelium cells Gene Set From WikiPathways Pathways 2024 proteins participating in the GPR143 in melanocytes and retinal pigment epithelium cells pathway from the WikiPathways Pathways 2024 dataset.
EPAC1 and PKA reduction of retinal inflammation Gene Set From WikiPathways Pathways 2024 proteins participating in the EPAC1 and PKA reduction of retinal inflammation pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis of A2E, implicated in retinal degradation Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways 2024 dataset.
establishment of blood-retinal barrier Gene Set From GO Biological Process Annotations 2025 genes participating in the establishment of blood-retinal barrier biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cone cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cone cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
all-trans retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the all-trans retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
11-cis-retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 11-cis-retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Retinal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary retinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal vascular disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal cell cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal cell cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal detachment Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal detachment in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal vascular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal lattice degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal lattice degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal detachment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal detachment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal perforation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute retinal necrosis syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute retinal necrosis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vascular occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Doyne honeycomb retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
late-onset retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease late-onset retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Branch retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Branch retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal dystrophy with leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal dystrophy with leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vasculopathy with cerebral leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vasculopathy with cerebral leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bothnia retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bothnia retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystrophies primarily involving the retinal pigment epithelium Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystrophies primarily involving the retinal pigment epithelium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal arterial tortuosity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal arterial tortuosity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Abnormal retinal correspondence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic disc anomalies with retinal and/or macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic disc anomalies with retinal and/or macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal microaneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal microaneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal hemangioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal hemangioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 3B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 3B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient retinal arterial occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient retinal arterial occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cobblestone retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cobblestone retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal pigment epithelium Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal pigment epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cone Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal cone from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal rod Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal rod from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal ganglion cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal ganglion cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal rod Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal rod in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal stem cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cone Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal ganglion cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal ganglion cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal microvascular endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal microvascular endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal dysplasia and retinal aplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal dysplasia and retinal aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-onset retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-onset retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal pigment epithelial atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early onset and severe retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset and severe retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal vasculopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal vasculopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-childhood-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic inherited retinal disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic inherited retinal disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal akinesia-cerebral and retinal hemorrhage syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia-cerebral and retinal hemorrhage syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmentary retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmentary retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Doyne honeycomb retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bothnia retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bothnia retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Patterned dystrophy of the retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Patterned dystrophy of the retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant rhegmatogenous retinal detachment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant rhegmatogenous retinal detachment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal cone dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal cone dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormality of retinal pigmentation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of retinal pigmentation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal retinal morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal retinal morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal capillary hemangioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal capillary hemangioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal vascular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal vascular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal arterial tortuosity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal arterial tortuosity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hearing loss and Retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing loss and Retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lattice retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lattice retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal detachment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal detachment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal dystrophy and obesity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal dystrophy and obesity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RP1-related retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RP1-related retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial retinal arterial macroaneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial retinal arterial macroaneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal detachment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central retinal vein equivalent Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal vein equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central retinal arteriolar equivalent Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal arteriolar equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal arteriolar caliber Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal arteriolar caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal vascular caliber Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Rhegmatogenous retinal detachment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal arteriolar tortuosity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal arteriolar tortuosity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Maximum retinal arteriolar tortuosity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum retinal arteriolar tortuosity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal venular tortuosity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal venular tortuosity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Maximum retinal venular tortuosity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum retinal venular tortuosity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal arteriole-to-venule ratio Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal arteriole-to-venule ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
ALL-TRANS-RETINAL Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ALL-TRANS-RETINAL drug from theDGIdb Drug Targets 2026 dataset.
13-CIS-RETINAL Gene Set From DGIdb Drug Targets 2026 interacting proteins for the 13-CIS-RETINAL drug from theDGIdb Drug Targets 2026 dataset.
11-CIS-RETINAL Gene Set From DGIdb Drug Targets 2026 interacting proteins for the 11-CIS-RETINAL drug from theDGIdb Drug Targets 2026 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital human immunodeficiency virus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 5, with tufting enteropathy, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vertical talus, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial paresis, hereditary congenital, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital glucose-galactose malabsorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aphakia, congenital primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital contractural arachnodactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nystagmus 6, congenital, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Afibrinogenemia, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 3, secretory sodium, congenital, syndromic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 3, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hypoplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital secretory diarrhea, chloride type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Indifference to pain, congenital, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital erythropoietic porphyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal recessive form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 6, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital cystic disease of liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital order of glycosylation type 1r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital ocular coloboma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital clubbing, isolated congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prothrombin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital aniridia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital hyperammonemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Partial congenital absence of teeth Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myasthenic syndrome, acetazolamide-responsive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glaucoma, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Hyperinsulinism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hyperinsulinism from the curated CTD Gene-Disease Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Congenital bilateral aplasia of vas deferens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.
Congenital Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Abnormalities from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Nonspherocytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 4 from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 4 from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Vertical talus, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertical talus, congenital from the curated CTD Gene-Disease Associations dataset.
Nystagmus 1, congenital, X- linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.
Facial paresis, hereditary, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.
Congenital anosmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital anosmia from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 5 from the curated CTD Gene-Disease Associations dataset.
Hyperferritinemia, hereditary, with congenital cataracts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.
Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Hernias, Diaphragmatic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hernias, Diaphragmatic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
Lethal Congenital Contracture Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Aphakia, congenital primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aphakia, congenital primary from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Nystagmus 2, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 3 from the curated CTD Gene-Disease Associations dataset.
Congenital contractural arachnodactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital contractural arachnodactyly from the curated CTD Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
Nystagmus 4, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Indifference to Pain, Congenital, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Ptosis, Hereditary Congenital 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset.
Pain Insensitivity, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital amegakaryocytic thrombocytopenia from the curated CTD Gene-Disease Associations dataset.
Adrenal Hyperplasia, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal Hyperplasia, Congenital from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.
Anemia, Hypoplastic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.
Congenital hypertrichosis lanuginosa Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital hypertrichosis lanuginosa from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 10 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 2 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, Compton-North Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 3 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital central hypoventilation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Zonular, with Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Lethal congenital contracture syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Microcoria, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcoria, congenital from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Congenital Retinal Fold Gene Set

falciform retinal fold Gene Set

Retinal Fold (Finding) Gene Set

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

retinal artery occlusion; retinal vein occlusion Gene Set

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

Retinal detachment or retinal break Gene Set

Retinal detachment with retinal break Gene Set

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

nonprogressive congenital retinal dystrophy Gene Set

congenital hypertrophy of retinal pigment epithelium Gene Set

retinal nonattachment, nonsyndromic congenital Gene Set

Congenital Hypertrophy Of Retinal Pigment Epithelium Gene Set

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

Congenital Amaurosis Of Retinal Origin Gene Set

Congenital Retinal Aneurysm Gene Set

fold Gene Set

morphogenesis of an epithelial fold Gene Set

neural fold formation Gene Set

neural fold bending Gene Set

neural fold elevation formation Gene Set

abnormality of the aryepiglottic fold Gene Set

prominent nasolabial fold Gene Set

thickened nuchal skin fold Gene Set

Kringle-like fold Gene Set

UBA/THIF-type NAD/FAD binding fold Gene Set

Ubiquitin-fold modifier 1 Gene Set

Rossmann-like alpha/beta/alpha sandwich fold Gene Set

Carbohydrate-binding-like fold Gene Set

Histone-fold Gene Set

Membrane-anchored ubiquitin-fold protein, HCG-1 Gene Set

Staphylococcal nuclease (SNase-like), OB-fold Gene Set

Ribosomal protein L30, ferredoxin-like fold domain Gene Set

Nucleolar GTP-binding protein 1, Rossman-fold domain Gene Set

ATP-grasp fold, subdomain 1 Gene Set

ATP-grasp fold, subdomain 2 Gene Set

Thioredoxin-like fold Gene Set

Alpha/Beta hydrolase fold Gene Set

Alpha/beta hydrolase fold-3 Gene Set

Alpha/beta hydrolase fold-1 Gene Set

Alpha/beta hydrolase fold-5 Gene Set

Immunoglobulin-like fold Gene Set

Phenylalanine-tRNA ligase, beta subunit, ferrodoxin-fold anticodon-binding Gene Set

Pectin lyase fold Gene Set

BTB/POZ fold Gene Set

Rad4/PNGase transglutaminase-like fold Gene Set

Peptidase C78, ubiquitin fold modifier-specific peptidase 1/ 2 Gene Set

ATP-grasp fold, succinyl-CoA synthetase-type Gene Set

Ubiquitin-fold modifier-conjugating enzyme 1 Gene Set

PAS fold Gene Set

Pectin lyase fold/virulence factor Gene Set

Flavodoxin-like fold Gene Set

ATP-grasp fold Gene Set

Ribosomal protein S5 domain 2-type fold, subgroup Gene Set

Nucleic acid-binding, OB-fold Gene Set

OB-fold nucleic acid binding domain, AA-tRNA synthetase-type Gene Set

PAS fold-3 Gene Set

RmlC-like jelly roll fold Gene Set

ATP-grasp fold, RimK-type Gene Set

RNA polymerase Rpb2, OB-fold Gene Set

Rubredoxin-type fold Gene Set

Tissue inhibitor of metalloproteinases-like, OB-fold Gene Set

C-type lectin fold Gene Set

LamG-like jellyroll fold Gene Set

Thiamin diphosphate-binding fold Gene Set

Ribosomal protein S5 domain 2-type fold Gene Set

Armadillo-type fold Gene Set

Plexin-like fold Gene Set

Clathrin, heavy chain/VPS, 7-fold repeat Gene Set

abnormal neural fold elevation formation Gene Set

abnormal cephalic neural fold morphology Gene Set

failure of head fold formation Gene Set

abnormal head fold morphology Gene Set

abnormal neural fold formation Gene Set

abnormal urogenital fold morphology Gene Set