Absence of visual evoked potentials

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Results for "Absence of visual evoked potentials": 464 gene sets

Name
absence of visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the absence of visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced amplitude of pattern visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal flash visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged flash visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the enlarged flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Abnormal Flash Visual Evoked Potentials Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Flash Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Timing Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Timing Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Undetectable Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Undetectable Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Enlarged Flash Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Flash Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormality of central somatosensory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of somatosensory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of vision evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal auditory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prolonged brainstem auditory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the prolonged brainstem auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Abnormality Of Somatosensory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Giant Somatosensory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Giant Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Lower-Limb Motor Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lower-Limb Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Central Somatosensory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Motor Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prolonged Brainstem Auditory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Brainstem Auditory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prolonged Somatosensory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
absent visual evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Abnormal Visual Evoked Potential Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Evoked Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal visual evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent visual evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
p300 potentials Gene Set From GAD Gene-Disease Associations genes associated with the disease p300 potentials in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
potentials Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term potentials in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
decreased amplitude of sensory action potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased amplitude of sensory action potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased miniature endplate potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased miniature endplate potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired ability to fire action potentials Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Decreased Miniature Endplate Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Miniature Endplate Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Amplitude Of Sensory Action Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Amplitude Of Sensory Action Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
impaired ability to fire action potentials Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
auditory evoked potential Gene Set From GAD Gene-Disease Associations genes associated with the disease auditory evoked potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
evoked Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term evoked in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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.
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.
absent linear vestibular evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reduced linear vestibular evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal linear vestibular evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Gaze-Evoked Horizontal Nystagmus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gaze-Evoked Horizontal Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Auditory Evoked Potential Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Auditory Evoked Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
reduced linear vestibular evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent linear vestibular evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal linear vestibular evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
evoked excitatory postsynaptic potential Gene Set From GO Biological Process Annotations 2025 genes participating in the evoked excitatory postsynaptic potential biological process from the curated GO Biological Process Annotations 2025 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.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin 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.
(ER)-localized multiprotein complex, in absence of Ig heavy chains Gene Set From CORUM Protein Complexes proteins in the (ER)-localized multiprotein complex, in absence of Ig heavy chains protein complex from the CORUM Protein Complexes dataset.
Absence of Tibia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Absence of Tibia from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Absence Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Absence from the curated CTD Gene-Disease Associations dataset.
juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anodontia; developmental absence of tooth Gene Set From GAD Gene-Disease Associations genes associated with the disease anodontia; developmental absence of tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood absence epilepsy. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital bilateral absence of the vas deferens Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital bilateral absence of the vas deferens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
absence Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term absence in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
absence of pectoralis minor muscle Gene Set From HPO Gene-Disease Associations genes associated with the absence of pectoralis minor muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital localized absence of skin Gene Set From HPO Gene-Disease Associations genes associated with the congenital localized absence of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of intrinsic factor Gene Set From HPO Gene-Disease Associations genes associated with the absence of intrinsic factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence seizures Gene Set From HPO Gene-Disease Associations genes associated with the absence seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of subcutaneous fat Gene Set From HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of bactericidal oxidative 'respiratory burst' in phagocytes Gene Set From HPO Gene-Disease Associations genes associated with the absence of bactericidal oxidative 'respiratory burst' in phagocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of lymph node germinal center Gene Set From HPO Gene-Disease Associations genes associated with the absence of lymph node germinal center phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of labia majora Gene Set From HPO Gene-Disease Associations genes associated with the absence of labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of secondary sex characteristics Gene Set From HPO Gene-Disease Associations genes associated with the absence of secondary sex characteristics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of subcutaneous fat over entire body except buttocks, hips, and thighs Gene Set From HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat over entire body except buttocks, hips, and thighs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of pubertal development Gene Set From HPO Gene-Disease Associations genes associated with the absence of pubertal development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
deficiency or absence of cytochrome b(-245) Gene Set From HPO Gene-Disease Associations genes associated with the deficiency or absence of cytochrome b(-245) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of renal corticomedullary differentiation Gene Set From HPO Gene-Disease Associations genes associated with the absence of renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of cd8+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the absence of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial absence of thumb Gene Set From HPO Gene-Disease Associations genes associated with the partial absence of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of stensen duct Gene Set From HPO Gene-Disease Associations genes associated with the absence of stensen duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of acoustic reflex Gene Set From HPO Gene-Disease Associations genes associated with the absence of acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of lutheran antigen on erythrocytes Gene Set From HPO Gene-Disease Associations genes associated with the absence of lutheran antigen on erythrocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) Gene Set From HPO Gene-Disease Associations genes associated with the nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Epilepsy, Absence Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Absence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
absence of ampa-mediated synaptic currents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of ampa-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence of nmda-mediated synaptic currents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of nmda-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence of all nails Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of all nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[tuberculin skin test reactivity, absence of] Gene Set From OMIM Gene-Disease Associations genes associated with the [tuberculin skin test reactivity, absence of] phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital bilateral absence of vas deferens Gene Set From OMIM Gene-Disease Associations genes associated with the congenital bilateral absence of vas deferens phenotype from the curated OMIM Gene-Disease Associations dataset.
ulna and fibula, absence of, with severe limb deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, childhood absence, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
Formation of HIV elongation complex in the absence of HIV Tat Gene Set From Reactome Pathways 2014 proteins participating in the Formation of HIV elongation complex in the absence of HIV Tat pathway from the Reactome Pathways dataset.
Abortive elongation of HIV-1 transcript in the absence of Tat Gene Set From Reactome Pathways 2014 proteins participating in the Abortive elongation of HIV-1 transcript in the absence of Tat pathway from the Reactome Pathways dataset.
Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Vas Deferens Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Spleen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Spleen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Muscle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Thymus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Germinal Epithelium Of Testes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Germinal Epithelium Of Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Kidneys Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Kidneys Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Septum Pellucidum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Septum Pellucidum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Both Testes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Both Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Absence Of Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Absence Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Parathyroid Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Parathyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Localized Absence Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Localized Absence Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Seizure Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Seizure Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of External Ear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Mandible Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Mandible in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Lung Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Unilateral Absence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Unilateral Absence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Absence Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Absence Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Tibia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Tibia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lacrimal Puncta, Absence Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Puncta, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Bladder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Uvula Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Alpha Granules Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Alpha Granules in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Jaw Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Jaw in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Diaphragm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Diaphragm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Lutheran Antigen On Erythrocytes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Lutheran Antigen On Erythrocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Tibia With Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Tibia With Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Absence Of Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Absence Of Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Breast With Absent Nipple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Breast With Absent Nipple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Penis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Penis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence, Atresia And Stricture Of Auditory Canal (External) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence, Atresia And Stricture Of Auditory Canal (External) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Part Of Brain Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Part Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Pulmonic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Pulmonic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atonic Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atonic Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Lymph Node Germinal Center Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Lymph Node Germinal Center in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pubertal Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pubertal Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Secondary Sex Characteristics Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Secondary Sex Characteristics in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Typical Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Typical Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Rib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Rib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Subcutaneous Fat Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Subcutaneous Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Intrinsic Factor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Intrinsic Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Cd8-Positive T Cells Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Cd8-Positive T Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vas Deferens, Congenital Bilarteral, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vas Deferens, Congenital Bilarteral, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Labia Majora Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Labia Majora in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stomach Bubble On Fetal Sonography Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stomach Bubble On Fetal Sonography in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fingerprints, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fingerprints, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Bactericidal Oxidative Respiratory Burst In Phagocytes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Bactericidal Oxidative Respiratory Burst In Phagocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Deficiency Or Absence Of Cytochrome B(-245) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deficiency Or Absence Of Cytochrome B(-245) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pain Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Acoustic Reflex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Acoustic Reflex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Attacks Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Attacks in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stensen Duct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stensen Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Islets Of Langerhans, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Islets Of Langerhans, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Absence Of Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Absence Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Renal Corticomedullary Differentiation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Renal Corticomedullary Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pectoralis Minor Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pectoralis Minor Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Absence Of Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Absence Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2023 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2023 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
absence seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of NMDA-mediated synaptic currents Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of NMDA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of all nails Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of all nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of AMPA-mediated synaptic currents Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of AMPA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Abortive elongation of HIV-1 transcript in the absence of Tat Gene Set From Reactome Pathways 2024 proteins participating in the Abortive elongation of HIV-1 transcript in the absence of Tat pathway from the Reactome Pathways 2024 dataset.
Caspase activation via Dependence Receptors in the absence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the Caspase activation via Dependence Receptors in the absence of ligand pathway from the Reactome Pathways 2024 dataset.
Formation of HIV elongation complex in the absence of HIV Tat Gene Set From Reactome Pathways 2024 proteins participating in the Formation of HIV elongation complex in the absence of HIV Tat pathway from the Reactome Pathways 2024 dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2025 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2025 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bilateral absence of vas deferens from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bilateral absence of vas deferens in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked congenital bilateral absence of vas deferens Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked congenital bilateral absence of vas deferens in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Absence of the sacrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Absence of the sacrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral absence of vas deferens phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Typical absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Typical absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anterolateral visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Visual areas Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Visual areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
IZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
visual signal transduction Gene Set From Biocarta Pathways proteins participating in the visual signal transduction pathway from the Biocarta Pathways dataset.
Visual Cortex Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Visual Cortex in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual cortex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual cortex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual pathway disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual pathway disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease visual disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual cortex Gene Set From GAD Gene-Disease Associations genes associated with the disease visual cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual field defects Gene Set From GAD Gene-Disease Associations genes associated with the disease visual field defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term visual in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
visual behavior Gene Set From GO Biological Process Annotations 2015 genes participating in the visual behavior biological process from the curated GO Biological Process Annotations 2015 dataset.
visual learning Gene Set From GO Biological Process Annotations 2015 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2015 dataset.
visual perception Gene Set From GO Biological Process Annotations 2015 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2015 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2015 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2015 dataset.
visual cortex disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease visual cortex disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
visual pathway disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease visual pathway disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
progressive visual field defects Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual auras Gene Set From HPO Gene-Disease Associations genes associated with the visual auras phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mildly reduced visual acuity Gene Set From HPO Gene-Disease Associations genes associated with the mildly reduced visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sudden central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow decrease in visual acuity Gene Set From HPO Gene-Disease Associations genes associated with the slow decrease in visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual hallucinations Gene Set From HPO Gene-Disease Associations genes associated with the visual hallucinations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cortical visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the cortical visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual loss Gene Set From HPO Gene-Disease Associations genes associated with the visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral visual field loss Gene Set From HPO Gene-Disease Associations genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
constricted visual fields Gene Set From HPO Gene-Disease Associations genes associated with the constricted visual fields phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large central visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Visual Perception Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Visual Perception phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pattern Recognition, Visual Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pattern Recognition, Visual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
the visual cycle I (vertebrates) Gene Set From HumanCyc Pathways proteins participating in the the visual cycle I (vertebrates) pathway from the HumanCyc Pathways 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.
abnormal visual acuity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual pursuit Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual pursuit phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased visual acuity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Visual signal transduction: Cones Gene Set From PID Pathways proteins participating in the Visual signal transduction: Cones pathway from the PID Pathways dataset.
Visual signal transduction: Rods Gene Set From PID Pathways proteins participating in the Visual signal transduction: Rods pathway from the PID Pathways dataset.
Diseases associated with visual transduction Gene Set From Reactome Pathways 2014 proteins participating in the Diseases associated with visual transduction pathway from the Reactome Pathways dataset.
Visual phototransduction Gene Set From Reactome Pathways 2014 proteins participating in the Visual phototransduction pathway from the Reactome Pathways dataset.
visual cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue visual cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Visual Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Illusions, Visual Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Illusions, Visual in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Pathway Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Pathway Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Auras Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Auras in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Cortex Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Cortex Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory And Visual Hallucinations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory And Visual Hallucinations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unspecified Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unspecified Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Field Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Field Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cortical Visual Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Visual Field Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Visual Field Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Loss Of Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Loss Of Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity, No Light Perception Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity, No Light Perception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Phenomena Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Phenomena in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Flasher - Visual Manifestation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flasher - Visual Manifestation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Glaucomatous Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glaucomatous Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Field Test Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Field Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow Decrease In Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Decrease In Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Accommodation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Accommodation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Field Defects Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Field Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Agnosia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Agnosia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Fixation Instability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Fixation Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Discomfort Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Discomfort in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mildly Reduced Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mildly Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tunnel Visual Field Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tunnel Visual Field Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Large Central Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity Light Perception With Projection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity Light Perception With Projection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonprogressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity Test Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity Test Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Best Corrected Visual Acuity Test Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Best Corrected Visual Acuity Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Visual Behavior For Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Visual Behavior For Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Fixation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Impairment And Blindness (Excl Colour Blindness) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment And Blindness (Excl Colour Blindness) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
visual perception Gene Set From GO Biological Process Annotations 2023 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2023 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2023 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2023 dataset.
visual learning Gene Set From GO Biological Process Annotations 2023 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2023 dataset.
visual system development Gene Set From GO Biological Process Annotations 2023 genes participating in the visual system development biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased visual acuity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual pursuit Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual pursuit phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual contrast sensitivity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual contrast sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Oligodendrocyte_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Oligodendrocyte precursor cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte precursor cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 2 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 2 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Leptomeningeal cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Leptomeningeal cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
B cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the B cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Vascular cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Vascular cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Microglial cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Microglial cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Astrocyte_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Astrocyte_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 3 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 3 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 4 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 4 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
GABAergic neuron_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the GABAergic neuron_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Endothelial cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Endothelial cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Defective visual phototransduction due to ABCA4 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to LRAT loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1LW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1MW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1SW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH12 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH5 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to STRA6 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset.
Diseases associated with visual transduction Gene Set From Reactome Pathways 2024 proteins participating in the Diseases associated with visual transduction pathway from the Reactome Pathways 2024 dataset.
Visual phototransduction Gene Set From Reactome Pathways 2024 proteins participating in the Visual phototransduction pathway from the Reactome Pathways 2024 dataset.
visual perception Gene Set From GO Biological Process Annotations 2025 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2025 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2025 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2025 dataset.
visual learning Gene Set From GO Biological Process Annotations 2025 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2025 dataset.
visual system development Gene Set From GO Biological Process Annotations 2025 genes participating in the visual system development biological process from the curated GO Biological Process Annotations 2025 dataset.
Visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual cortex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual cortex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual pathway disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual pathway disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Visual cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Visual impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral visual field loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral visual field loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral visual impairment and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral visual impairment and intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical surface area (visual PC2) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (visual PC2) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
perceptual and visual search speed (trail making test A) (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the perceptual and visual search speed (trail making test A) (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic maculopathy with decreased visual acuity in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic maculopathy with decreased visual acuity in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

absence of visual evoked potentials Gene Set

reduced amplitude of pattern visual evoked potentials Gene Set

abnormal flash visual evoked potentials Gene Set

enlarged flash visual evoked potentials Gene Set

Abnormal Flash Visual Evoked Potentials Gene Set

Abnormal Timing Of Pattern Reversal Visual Evoked Potentials Gene Set

Undetectable Visual Evoked Potentials Gene Set

Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials Gene Set

Enlarged Flash Visual Evoked Potentials Gene Set

abnormality of central somatosensory evoked potentials Gene Set

abnormality of somatosensory evoked potentials Gene Set

abnormality of vision evoked potentials Gene Set

abnormal auditory evoked potentials Gene Set

prolonged brainstem auditory evoked potentials Gene Set

Abnormality Of Somatosensory Evoked Potentials Gene Set

Giant Somatosensory Evoked Potentials Gene Set

Abnormal Lower-Limb Motor Evoked Potentials Gene Set

Abnormality Of Central Somatosensory Evoked Potentials Gene Set

Abnormal Motor Evoked Potentials Gene Set

Prolonged Brainstem Auditory Evoked Potentials Gene Set

Prolonged Somatosensory Evoked Potentials Gene Set

absent visual evoked potential Gene Set

abnormal visual evoked potential Gene Set

Abnormal Visual Evoked Potential Gene Set

abnormal visual evoked potential Gene Set

absent visual evoked potential Gene Set

p300 potentials Gene Set

potentials Gene Set

decreased amplitude of sensory action potentials Gene Set

decreased miniature endplate potentials Gene Set

impaired ability to fire action potentials Gene Set

Decreased Miniature Endplate Potentials Gene Set

Decreased Amplitude Of Sensory Action Potentials Gene Set

impaired ability to fire action potentials Gene Set

auditory evoked potential Gene Set

evoked Gene Set

gaze-evoked horizontal nystagmus Gene Set

gaze-evoked nystagmus Gene Set

absent linear vestibular evoked potential Gene Set

reduced linear vestibular evoked potential Gene Set

abnormal linear vestibular evoked potential Gene Set

Gaze-Evoked Horizontal Nystagmus Gene Set

Abnormal Auditory Evoked Potential Gene Set

reduced linear vestibular evoked potential Gene Set

absent linear vestibular evoked potential Gene Set

abnormal linear vestibular evoked potential Gene Set

evoked excitatory postsynaptic potential Gene Set

Congenital absence of salivary gland Gene Set

Ulna and fibula absence of with severe limb deficiency Gene Set

Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set

Partial congenital absence of teeth Gene Set

(ER)-localized multiprotein complex, in absence of Ig heavy chains Gene Set

Absence of Tibia Gene Set

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

Epilepsy, Absence Gene Set

juvenile absence epilepsy Gene Set

childhood absence epilepsy Gene Set

early onset absence epilepsy Gene Set

anodontia; developmental absence of tooth Gene Set

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

childhood absence epilepsy. Gene Set

epilepsy, absence; epilepsy, generalized Gene Set

congenital bilateral absence of the vas deferens Gene Set

absence Gene Set

positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

positive regulation of collateral sprouting in absence of injury Gene Set

extrinsic apoptotic signaling pathway in absence of ligand Gene Set

collateral sprouting in absence of injury Gene Set

regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

signal transduction in absence of ligand Gene Set

negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

negative regulation of collateral sprouting in absence of injury Gene Set

regulation of collateral sprouting in absence of injury Gene Set

negative regulation of signal transduction in absence of ligand Gene Set

absence of pectoralis minor muscle Gene Set

congenital localized absence of skin Gene Set

absence of intrinsic factor Gene Set

absence seizures Gene Set

absence of subcutaneous fat Gene Set