Name

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.

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.

nucleus of the diagonal band, left, vertical division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in nucleus of the diagonal band, left, vertical division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

vertical nucleus of the diagonal band Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in vertical nucleus of the diagonal band relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles 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.

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.

vertical Gene Set

From GeneRIF Biological Term Annotations

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

Vertical cup-disc ratio Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Vertical cup-disc ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

vertical supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

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

vertical clivus Gene Set

From HPO Gene-Disease Associations

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

increased vertical activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vertical activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertical vestibuloocular reflex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertical vestibuloocular reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased vertical stereotypic behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vertical stereotypic behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vertical activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vertical activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertical activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertical activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertical talus, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the vertical talus, congenital phenotype from the curated OMIM 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.

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.

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.

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.