Name

spontaneous ocular nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spontaneous ocular nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular toxoplasmosis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

X-linked infantile nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype 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.

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.

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.

Episodic ataxia with nystagmus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic ataxia with nystagmus from the curated CTD Gene-Disease Associations dataset.

Nystagmus, Pathologic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus, Pathologic from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Nystagmus 3, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 3, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Nystagmus, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus, Congenital from the curated CTD Gene-Disease Associations dataset.

vestibular nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign paroxysmal positional nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease benign paroxysmal positional nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pathologic nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dissociated nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

nystagmus Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term nystagmus in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

horizontal nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the horizontal nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nystagmus-induced head nodding Gene Set

From HPO Gene-Disease Associations

genes associated with the nystagmus-induced head nodding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gaze-evoked horizontal nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the gaze-evoked horizontal nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

rotary nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the rotary nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

horizontal pendular nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the horizontal pendular nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gaze-evoked nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the gaze-evoked nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pendular nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the pendular nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertical nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the vertical nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

downbeat nystagmus Gene Set

From HPO Gene-Disease Associations

genes associated with the downbeat nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nystagmus 2, congenital, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 2, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 7, congenital, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 7, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus, infantile periodic alternating, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 1, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 1, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 3, congenital, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 3, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 6, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 6, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 5, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 5, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 4, congenital, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 4, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Pneumothorax, primary spontaneous Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pneumothorax, primary spontaneous phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pneumothorax, Primary Spontaneous Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pneumothorax, Primary Spontaneous from the curated CTD Gene-Disease Associations dataset.

Abortion, Spontaneous Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abortion, Spontaneous from the curated CTD Gene-Disease Associations dataset.

abortion, spontaneous; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b; hepatitis b, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b; hepatitis b, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical artery dissection, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical artery dissection, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

remission, spontaneous; retinopathy of prematurity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease remission, spontaneous; retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous preterm birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spontaneous preterm birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous chromosomal instability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spontaneous chromosomal instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent spontaneous miscarriages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrent spontaneous miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; coronary artery disease; rupture, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; coronary artery disease; rupture, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abortion, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abortion, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous abortion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spontaneous abortion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent spontaneous abortion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrent spontaneous abortion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abortion, spontaneous; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abortion, spontaneous; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous preterm delivery. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spontaneous preterm delivery. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term spontaneous in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

lack of spontaneous play Gene Set

From HPO Gene-Disease Associations

genes associated with the lack of spontaneous play phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous pneumothorax Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous esophageal perforation Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous esophageal perforation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous hematomas Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous hematomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous abortion Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent spontaneous abortion Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous, recurrent epistaxis Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous, recurrent epistaxis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous neonatal pneumothorax Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous neonatal pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous hemolytic crises Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous hemolytic crises phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Abortion, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Abortion, Spontaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Spontaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Rupture, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Rupture, Spontaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

spontaneous chromosome breakage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spontaneous chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spontaneous skin ulceration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spontaneous skin ulceration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

no spontaneous movement Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the no spontaneous movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pneumothorax, primary spontaneous Gene Set

From OMIM Gene-Disease Associations

genes associated with the pneumothorax, primary spontaneous phenotype from the curated OMIM Gene-Disease Associations dataset.

Ocular coloboma, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ocular coloboma, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ocular albinism, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ocular albinism, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomagnesemia 5, renal, with ocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomagnesemia 5, renal, with ocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities 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.

STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cystinosis, ocular nonnephropathic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cystinosis, ocular nonnephropathic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ocular Albinism type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ocular Albinism type 1 from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Ocular Hypertension Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ocular Hypertension from the curated CTD Gene-Disease Associations dataset.

Hypomagnesemia 5, Renal, with Ocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomagnesemia 5, Renal, with Ocular Involvement from the curated CTD Gene-Disease Associations dataset.

Ocular Motility Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ocular Motility Disorders from the curated CTD Gene-Disease Associations dataset.

Albinism ocular late onset sensorineural deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism ocular late onset sensorineural deafness from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Cystinosis, ocular nonnephropathic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cystinosis, ocular nonnephropathic from the curated CTD Gene-Disease Associations dataset.

Stickler Syndrome, Type I, Nonsyndromic Ocular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler Syndrome, Type I, Nonsyndromic Ocular from the curated CTD Gene-Disease Associations dataset.

Ocular Physiological Phenomena Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Ocular Physiological Phenomena in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

ocular motility disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ocular motility disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ocular albinism Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ocular albinism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ocular cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ocular cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ocular motility disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular hypotension Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular albinism Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular hyperemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular hypertension Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ocular melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

radiation-induced ocular telangiectasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease radiation-induced ocular telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular cicatricial pemphigoid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular cicatricial pemphigoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular histoplasmosis syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular histoplasmosis syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular albinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular albinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bradycardia; glaucoma, open-angle; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bradycardia; glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioretinitis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioretinitis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

classical ocular phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease classical ocular phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; ocular motility disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; ocular motility disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

refractive error and ocular biometrics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease refractive error and ocular biometrics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leber congenital amaurosis and a normal ocular phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leber congenital amaurosis and a normal ocular phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; low tension glaucoma; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; low tension glaucoma; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular physiological phenomena Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular physiological phenomena in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ocular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

abnormal vestibulo-ocular reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of ocular abduction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of ocular abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired ocular adduction Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ocular adduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

jerky ocular pursuit movements Gene Set

From HPO Gene-Disease Associations

genes associated with the jerky ocular pursuit movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired ocular abduction Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ocular abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ocular albinism Gene Set

From HPO Gene-Disease Associations

genes associated with the ocular albinism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ocular region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ocular region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of ocular smooth pursuit Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of ocular smooth pursuit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ocular pain Gene Set

From HPO Gene-Disease Associations

genes associated with the ocular pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ocular Hypertension Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ocular Hypertension phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ocular Motility Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ocular Motility Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Albinism, Ocular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Albinism, Ocular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ocular albinism protein, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ocular albinism protein, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ocular pterygium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular pterygium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular hypertelorism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular hypertelorism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular rupture Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular rupture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ocular fundus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ocular fundus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular distichiasis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular distichiasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular hypotension Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular hypotension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular hypertension Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular albinism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular albinism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ocular hypotelorism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ocular hypotelorism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomagnesemia 5, renal, with ocular involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomagnesemia 5, renal, with ocular involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

ocular albinism, type i, nettleship-falls type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ocular albinism, type i, nettleship-falls type phenotype from the curated OMIM Gene-Disease Associations dataset.

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.

?coloboma, ocular, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?coloboma, ocular, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ocular albinism with sensorineural deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the ocular albinism with sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler sydrome, type i, nonsyndromic ocular Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler sydrome, type i, nonsyndromic ocular phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome/ocular albinism, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome/ocular albinism, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-ocular apraxia-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-ocular apraxia-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular phenotype from the curated OMIM Gene-Disease Associations dataset.

cystinosis, ocular nonnephropathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystinosis, ocular nonnephropathic phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis, proximal, with ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, proximal, with ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal opacification and other ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.