| Name |
|---|
Severe Recurrent Major Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Recurrent Major Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
major mood disorders: bipolar, major depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major mood disorders: bipolar, major depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Broad depression or major depressive disorder (recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or major depressive disorder (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe Major Depression With Psychotic Features Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Major Depression With Psychotic Features in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
neuroticism, major depression, and anxiety disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuroticism, major depression, and anxiety disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Major Depression, Single Episode Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Depression, Single Episode in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Remission after antidepressant treatment in major depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Remission after antidepressant treatment in major depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Nicotine dependence and major depression (severity of comorbidity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nicotine dependence and major depression (severity of comorbidity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Remission after SSRI treatment in major depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Remission after SSRI treatment in major depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Broad depression or major depressive disorder (self-reported) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or major depressive disorder (self-reported) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to ketamine in bipolar disorder or major depression (antidepressant effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ketamine in bipolar disorder or major depression (antidepressant effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to ketamine in bipolar disorder or major depression (dissociation effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ketamine in bipolar disorder or major depression (dissociation effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder and major depressive episode treated with electroconvulsive therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder and major depressive episode treated with electroconvulsive therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Recurrent Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Major Depressive Episodes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Major Depressive Episodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Recurrent major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or recurrent major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
severe recurrent varicella Gene SetFrom HPO Gene-Disease Associations genes associated with the severe recurrent varicella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Varicella, Severe Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Varicella, Severe Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontonasal Dysplasia, Severe Microphthalmia, Severe Facial Clefting Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontonasal Dysplasia, Severe Microphthalmia, Severe Facial Clefting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Erosive tooth wear (severe vs non-severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erosive tooth wear (severe vs non-severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Depression in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
mental depression Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease mental depression in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
mental depression Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mental depression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endogenous depression Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endogenous depression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
repiratory depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease repiratory depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia ; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia ; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety and hostility and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression, psychosis and antipsychotic response Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression, psychosis and antipsychotic response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; manic depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; manic depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
suicide; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease suicide; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; depression; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; depression; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; personality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; personality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; alcoholism; depression; narcolepsy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcoholism; depression; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia ; depression ; bipolar disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia ; depression ; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression in parkinson's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression in parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid levels; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid levels; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; neuroticism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression and response to antidepressant treatment Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression and response to antidepressant treatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressed suicide; suicide due to depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression, postpartum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression, postpartum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression, postpartum; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression, postpartum; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bipolar disorder; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bipolar disorder; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; treatment with fluoxetine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; treatment with fluoxetine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression, postpartum; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression, postpartum; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; thrombocyte mao activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; thrombocyte mao activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aura anxiety and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aura anxiety and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; bipolar disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term depression in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Schizophrenia, bipolar disorder and depression (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia, bipolar disorder and depression (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Suicidal ideation in depression or bipolar disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Suicidal ideation in depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Depression (quantitative trait) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Depression (quantitative trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Suicide attempts in depression or bipolar disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Suicide attempts in depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
mental depression Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease mental depression in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
endogenous depression Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease endogenous depression in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
depression Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the depression phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
depression Gene SetFrom HPO Gene-Disease Associations genes associated with the depression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Depression, Postpartum Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Depression, Postpartum phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
long term depression Gene SetFrom KEGG Pathways proteins participating in the long term depression pathway from the KEGG Pathways dataset. |
absent long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased synaptic depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased synaptic depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal depression-related behavior Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal depression-related behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal synaptic depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{unipolar depression, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {unipolar depression, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
depression Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term depression in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mental Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mental Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Unipolar Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Unipolar Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Depression (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Depression (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Post Stroke Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Post Stroke Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endogenous Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endogenous Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Clinical Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Clinical Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bone Marrow Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Marrow Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Perinatal Depression In Mother Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Depression In Mother in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Menopausal Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Menopausal Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Involutional Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Involutional Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Winter Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Winter Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mild Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mild Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metopic Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metopic Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Depression Anxiety Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Depression Anxiety Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reactive Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reactive Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Moderate Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Moderate Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Circulatory Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Circulatory Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Depression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
H/O: Depression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype H/O: Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Respiratory Depression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
St Segment Depression (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype St Segment Depression (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fh: Depression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fh: Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unipolar Depression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unipolar Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
positive regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
absent long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased synaptic depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased synaptic depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal synaptic depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synaptic depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased synaptic depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased synaptic depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal depression-related behavior Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal depression-related behavior phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Vitamin D sensitive calcium signaling in depression Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Vitamin D sensitive calcium signaling in depression pathway from the WikiPathways Pathways 2024 dataset. |
positive regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset. |
Melancholic depression Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Melancholic depression in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Melancholic depression Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Melancholic depression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Postpartum depression Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Postpartum depression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Depression Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Depression phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cognitive impairment in depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive impairment in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression x herpes simplex 1 infection interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression x herpes simplex 1 infection interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to esketamine in treatment resistant depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to esketamine in treatment resistant depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to esketamine (responder status) in treatment resistant depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to esketamine (responder status) in treatment resistant depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to selective serotonin reuptake inhibitors in depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to selective serotonin reuptake inhibitors in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to bupropion and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to bupropion and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to citalopram or escitalopram in depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to citalopram or escitalopram in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to selective serotonin reuptake inhibitors and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to selective serotonin reuptake inhibitors and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to antidepressants in depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antidepressants in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-response to citalopram or escitalopram and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-response to citalopram or escitalopram and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to citalopram or escitalopram and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to citalopram or escitalopram and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-response to antidepressants and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-response to antidepressants and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-response to selective serotonin reuptake inhibitors and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-response to selective serotonin reuptake inhibitors and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-response to bupropion and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-response to bupropion and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to antidepressants and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antidepressants and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to bupropion in depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to bupropion in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to serotonin reuptake inhibitors in non-psychotic unipolar depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to serotonin reuptake inhibitors in non-psychotic unipolar depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis (pre-diagnosis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (pre-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis (post-diagnosis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (post-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in smokers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Suicide attempts in depression or bipolar disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicide attempts in depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Seasonality and depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Seasonality and depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression (quantitative trait) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression (quantitative trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder and depression (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder and depression (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in response to interferon-based therapy in chronic hepatitis C Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in response to interferon-based therapy in chronic hepatitis C phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Broad depression or bipolar disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Broad depression or schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Treatment resistant depression Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Treatment resistant depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression x maternal smoking during pregnancy interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression x maternal smoking during pregnancy interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Long-term depression Gene SetFrom KEGG Pathways 2026 proteins participating in the Long-term depression pathway from the KEGG Pathways 2026 dataset. |
island of Calleja major Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in island of Calleja major relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Major island of Calleja Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Major island of Calleja relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Beta thalassemia major Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Beta thalassemia major phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
viral capsid, major subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the viral capsid, major subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
virus tail, major subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the virus tail, major subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Major Affective Disorder 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 8 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 9 from the curated CTD Gene-Disease Associations dataset. |
Depressive Disorder, Major Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Depressive Disorder, Major from the curated CTD Gene-Disease Associations dataset. |
Major Depressive Disorder 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 1 from the curated CTD Gene-Disease Associations dataset. |
Major Depressive Disorder 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 2 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 4 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 2 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 3 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 1 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 6 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 7 from the curated CTD Gene-Disease Associations dataset. |
Major Affective Disorder 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 5 from the curated CTD Gene-Disease Associations dataset. |
Depressive Disorder, Major Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Depressive Disorder, Major in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
major depressive disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease major depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
variola major Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease variola major in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
depressive disorder, major; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; depressive disorder, major Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta-thalassemia major Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta-thalassemia major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; bipolar disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major and bipolar depressives Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major and bipolar depressives in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major depressive disorder (broad) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major depressive disorder (broad) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; depressive disorder, major; panic disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
two major non-ribosomal nucleolar proteins and its implication Gene SetFrom GAD Gene-Disease Associations genes associated with the disease two major non-ribosomal nucleolar proteins and its implication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major psychoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major trauma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major depressive disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major depressive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major psychiatric disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major depressive disorder and panic disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease major depressive disorder and panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; nausea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; nausea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complications after major abdominal operations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complications after major abdominal operations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; depressive disorder, major Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive episode, major Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive episode, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; bipolar disorder; affective psychoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; bipolar disorder; suicide Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; depressive disorder, major; bipolar disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; suicide Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressive disorder, major; phobia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; phobia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; depressive disorder, major; neuroticism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
major Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term major in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Anxiety and major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Anxiety and major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Major depressive disorder (broad) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Major depressive disorder (broad) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Anxiety in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Anxiety in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Major mood disorders Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Major mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Bipolar disorder and major depressive disorder (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder and major depressive disorder (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
major depressive disorder Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease major depressive disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
pectoralis major hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoralis major hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the pectoralis major muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the pectoralis major muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Depressive Disorder, Major Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Depressive Disorder, Major phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Major intrinsic protein, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major intrinsic protein, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major facilitator superfamily associated domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major facilitator superfamily associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major facilitator superfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major facilitator superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major vault protein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major vault protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major facilitator superfamily domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major facilitator superfamily domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Eosinophil major basic protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Eosinophil major basic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin/major histocompatibility complex, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin/major histocompatibility complex, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major prion protein N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major prion protein N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pyridoxal phosphate-dependent transferase, major region, subdomain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxal phosphate-dependent transferase, major region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pyridoxal phosphate-dependent transferase, major region, subdomain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxal phosphate-dependent transferase, major region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major intrinsic protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major intrinsic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major urinary protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major urinary protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
decreased urine major urinary protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased urine major urinary protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
multiple major aortopulmonary collateral arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased urine major urinary protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased urine major urinary protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal major salivary gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal major salivary gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{major affective disorder 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major depressive disorder, response to citalopram therapy in} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major depressive disorder, response to citalopram therapy in} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder-8, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder-8, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
major affective disorder 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the major affective disorder 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder-7, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder-7, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?major affective disorder 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?major affective disorder 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder 3, early onset} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset. |
major depressive disorder 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the major depressive disorder 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
major depressive disorder 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the major depressive disorder 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major affective disorder-9, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major affective disorder-9, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{major depressive disorder and accelerated response to antidepressant drug treatment} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {major depressive disorder and accelerated response to antidepressant drug treatment} phenotype from the curated OMIM Gene-Disease Associations dataset. |
mRNA Splicing - Major Pathway Gene Setproteins participating in the mRNA Splicing - Major Pathway pathway from the Reactome Pathways dataset. |
major vestibular gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue major vestibular gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
psoas major Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue psoas major in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Major Depressive Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Affective Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Affective Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Psychiatric Illness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Psychiatric Illness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Salivary Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Salivary Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Variola Major Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Variola Major in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Pectoralis Major Muscle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Pectoralis Major Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Congenital Anomaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Congenital Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Histocompatibility Complex Class Ii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Histocompatibility Complex Class Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Neurocognitive Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Major Neurocognitive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Major Depressive Disorder, Increased Recurrence Of Depressive Episodes In, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Major Depressive Disorder, Increased Recurrence Of Depressive Episodes In, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pectoralis Major Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pectoralis Major Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Withdrawal-Induced Major Motor Seizure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Withdrawal-Induced Major Motor Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal major salivary gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal major salivary gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased urine major urinary protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased urine major urinary protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased urine major urinary protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased urine major urinary protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
multiple major aortopulmonary collateral arteries Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Major receptors targeted by epinephrine and norepinephrine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Major receptors targeted by epinephrine and norepinephrine pathway from the WikiPathways Pathways 2024 dataset. |
Major pathway of rRNA processing in the nucleolus and cytosol Gene Setproteins participating in the Major pathway of rRNA processing in the nucleolus and cytosol pathway from the Reactome Pathways 2024 dataset. |
mRNA Splicing - Major Pathway Gene Setproteins participating in the mRNA Splicing - Major Pathway pathway from the Reactome Pathways 2024 dataset. |
Major depressive disorder Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Major depressive disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Variola major Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Variola major in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Major depressive disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Major depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
beta-thalassemia major Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease beta-thalassemia major in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Psoas major Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Psoas major in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Major vestibular gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Major vestibular gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Major mitochondrial derivative Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Major mitochondrial derivative cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Major depressive disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Major depressive disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Beta-thalassemia major Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Beta-thalassemia major phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypersomnia during a major depressive episode in bipolar disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypersomnia during a major depressive episode in bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Suicide ideation score in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicide ideation score in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Suicide attempts in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicide attempts in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder (stressful life events interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder (stressful life events interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to cognitive-behavioural therapy in anxiety and major depressive disorders Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in anxiety and major depressive disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to cognitive-behavioural therapy in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to serotonin reuptake inhibitors in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to serotonin reuptake inhibitors in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive episode treated with electroconvulsive therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive episode treated with electroconvulsive therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder (MTAG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to anti-depressant treatment in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-depressant treatment in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder (broad) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder (broad) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major mood disorders Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bipolar disorder or major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder (unexposed to adversity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder (unexposed to adversity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major coronary event in placebo-treated cardiovascular disease (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major coronary event in placebo-treated cardiovascular disease (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major coronary event in cardiovascular disease (time to event) (darapladib treatment interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major coronary event in cardiovascular disease (time to event) (darapladib treatment interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Duloxetine response in major depressive disorder (% change in symptom score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Duloxetine response in major depressive disorder (% change in symptom score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Placebo response in major depressive disorder (% change in symptom score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Placebo response in major depressive disorder (% change in symptom score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma kynurenine levels in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma kynurenine levels in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma kynurenine to tryptophan ratio in major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma kynurenine to tryptophan ratio in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depressive symptom measurement or major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depressive symptom measurement or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma and major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Stress sensitivity (neuroticism score x major depressive disorder status interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress sensitivity (neuroticism score x major depressive disorder status interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoglobinuria, acute recurrent, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign recurrent intrahepatic cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hydatidiform mole, recurrent, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hydatidiform mole, recurrent, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
recurrent axon collateral Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Hypotrichosis And Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset. |
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset. |
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset. |
Vertigo, Benign Recurrent, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vertigo, Benign Recurrent, 2 from the curated CTD Gene-Disease Associations dataset. |
recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
recurrent hypersomnia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
idiopathic recurrent miscarriage. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent bacterial infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent bacterial infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory papillomatosis, juvenile-onset; recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic recurrent miscarriages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent cardiovascular event Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent cardiovascular event in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent spontaneous miscarriages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; coagulation disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; rhinitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent abortions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent abortions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent aphthous stomatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent aphthous stomatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal cord infarction and recurrent venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; in vitro fertilization success Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent spontaneous abortion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous abortion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent oral ulcers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent oral ulcers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal loss, late; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent early fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent deep-vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent deep-vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent or chronic idiopathic pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent acute pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent acute pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
herpes-associated recurrent lymphocytic meningitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease herpes-associated recurrent lymphocytic meningitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent respiratory infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent respiratory infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent respiratory papillomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent respiratory papillomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent pregnancy loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term recurrent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
recurrent hypersomnia Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease recurrent hypersomnia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
recurrent viral infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent viral infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent mycobacterial infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent mycobacterium avium complex infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterium avium complex infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent bacterial infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent bacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent aspergillus infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aspergillus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent abscess formation Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mandibular subluxations Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mandibular subluxations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent fungal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent staphylococcal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent staphylococcal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pharyngitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pharyngitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent vulvovaginal candidiasis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent vulvovaginal candidiasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial meningitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pneumonia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent enteroviral infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent enteroviral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent thrombophlebitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent thrombophlebitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cerebral hemorrhage Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent aspiration pneumonia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aspiration pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent encephalopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent e. coli infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent e. coli infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mycobacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mycobacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent aphthous stomatitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aphthous stomatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pancreatitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pancreatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent loss of toenails and fingernails Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections in infancy and early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent otitis media Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent otitis media phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent meningitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent candida infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent candida infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent urinary tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent urinary tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
failure to thrive secondary to recurrent infections Gene SetFrom HPO Gene-Disease Associations genes associated with the failure to thrive secondary to recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cutaneous abscess formation Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cutaneous abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper and lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent burkholderia cepacia infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent burkholderia cepacia infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent spontaneous abortion Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent sinopulmonary infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent sinopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent klebsiella infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent klebsiella infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent systemic pyogenic infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent systemic pyogenic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent myoglobinuria Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent myoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent gram-negative bacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent gram-negative bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent corneal erosions Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent corneal erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections due to aspiration Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent respiratory infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent respiratory infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spontaneous, recurrent epistaxis Gene SetFrom HPO Gene-Disease Associations genes associated with the spontaneous, recurrent epistaxis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent singultus Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent singultus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent subcortical infarcts Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent subcortical infarcts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent skin infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bronchopulmonary infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bronchopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mycobacterium avium complex infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mycobacterium avium complex infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent hypoglycemia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent protozoan infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent protozoan infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent meningococcal disease Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent meningococcal disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent viral infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent viral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent sinusitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent sinusitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial skin infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent serratia marcescens infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent serratia marcescens infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent streptococcus pneumoniae infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent streptococcus pneumoniae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent neisserial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent neisserial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent deep vein thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent deep vein thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent opportunistic infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent opportunistic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bronchitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bronchitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent haemophilus influenzae infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent haemophilus influenzae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cutaneous fungal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cutaneous fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent staphylococcus aureus infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent staphylococcus aureus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hydatidiform mole, recurrent, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydatidiform mole, recurrent, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
?hypotrichosis and recurrent skin vesicles Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?hypotrichosis and recurrent skin vesicles phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyper-ige recurrent infection syndrome, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
invasive pneumococcal disease, recurrent isolated, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
invasive pneumococcal disease, recurrent isolated, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, benign recurrent intrahepatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, recurrent, with pressure palsies Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset. |
myoglobinuria, acute recurrent, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, benign recurrent intrahepatic, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyper-ige recurrent infection syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
vertigo, benign recurrent, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the vertigo, benign recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Recurrent Otitis Media Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Endometrial Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Endometrial Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ovarian Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Recurrent Intrahepatic Cholestasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Aphthous Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aphthous Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hepatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Genital Herpes Simplex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Genital Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Sinusitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Upper Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Seizure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hand Flapping Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hand Flapping in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Transformed Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Transformed Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Recurrent Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervix Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervix Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Locally Recurrent Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Locally Recurrent Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pterygium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pterygium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Brain Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Adult Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Desmoid-Type Fibromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Desmoid-Type Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cerebral Hemorrhage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Optic Neuritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Depressive Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bronchitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bronchitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chronic Lymphoid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Lymphoid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Adult Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hemophagocytic Lymphohistiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hemophagocytic Lymphohistiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Otitis Media Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Meningitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Papillomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Papillomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Peritonitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oesophageal Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Laryngeal Squamous Cell Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Squamous Cell Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult T-Cell Lymphoma/Leukaemia Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult T-Cell Lymphoma/Leukaemia Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Large B-Cell Lymphoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lung Adenocarcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lung Adenocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ovarian Serous Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Serous Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Atypical Teratoid/Rhabdoid Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oropharyngeal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oropharyngeal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Rectal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rectal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Dedifferentiated Liposarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Dedifferentiated Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Cell Lung Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Cell Lung Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Erosion Of Cornea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Erosion Of Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelial Recurrent Erosion Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Recurrent Myoglobinuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Recurrent Myoglobinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bacterial Meningitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Aspiration Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aspiration Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesothelioma Malignant Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma Malignant Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pyelonephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pyelonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Head And Neck Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Carcinoma Cell Type Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Carcinoma Cell Type Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Head And Neck Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Non-Squamous Non-Small Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Non-Squamous Non-Small Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Infections Due To Aspiration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Due To Aspiration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Larynx Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Larynx Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ewing'S Sarcoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ewing'S Sarcoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Infections Of The Middle Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Of The Middle Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infections, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infections, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Infection Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Laryngeal Nerve Paralysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Laryngeal Nerve Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cushing Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cushing Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Subcortical Infarcts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Subcortical Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intrahepatic Cholangiocarcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholangiocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Mouth Ulcers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Mouth Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Recurrent Pericarditis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Craniopharyngioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Proliferative Glomerulonephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Proliferative Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pulmonary Embolism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pulmonary Embolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Systemic Pyogenic Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Systemic Pyogenic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chordoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cystitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cystitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersomnia, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnia, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Salivary Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Small Lymphocytic Lymphoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Small Lymphocytic Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Biliary Tract Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cerebral Infarction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Plasma Cell Myeloma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Plasma Cell Myeloma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Salivary Gland Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Gland Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bacterial Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Thyroid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Labialis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Labialis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Anaplastic Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Respiratory Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Tumor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Fevers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fevers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spontaneous, Recurrent Epistaxis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous, Recurrent Epistaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bacterial Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Fungal Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fungal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Opportunistic Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Opportunistic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Viral Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mandibular Subluxations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mandibular Subluxations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infection Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infection Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Upper And Lower Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Lower Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Singultus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Singultus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Spontaneous Abortion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Spontaneous Abortion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Sinopulmonary Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Sinopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Cutaneous Abscess Formation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Cutaneous Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Enteroviral Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Enteroviral Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Meningococcal Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Meningococcal Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Neisserial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Neisserial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Failure To Thrive Secondary To Recurrent Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Failure To Thrive Secondary To Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abscess Formation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Candida Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Candida Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Gastroenteritis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Haemophilus Influenzae Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Haemophilus Influenzae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Streptococcus Pneumoniae Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Streptococcus Pneumoniae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bronchopulmonary Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Protozoan Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Protozoan Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Staphylococcus Aureus Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcus Aureus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Vulvovaginal Candidiasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Vulvovaginal Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections In Infancy And Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Myoglobinuria, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myoglobinuria, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Encephalopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Intrapulmonary Hemorrhage Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Intrapulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bacterial Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Headache Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Headache Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Aspergillus Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Aspergillus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Burkholderia Cepacia Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Burkholderia Cepacia Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Klebsiella Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Klebsiella Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Serratia Marcescens Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Serratia Marcescens Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mycobacterial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Paroxysmal Headache Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Paroxysmal Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Vomiting, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vomiting, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bronchiolitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchiolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Thrombophlebitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thrombophlebitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mycobacterium Avium Complex Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterium Avium Complex Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Hypoglycemia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Thromboembolism Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thromboembolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Viral Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Staphylococcal Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Gram-Negative Bacterial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gram-Negative Bacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Loss Of Toenails And Fingernails Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Loss Of Toenails And Fingernails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Pharyngitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Pharyngitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Deep Vein Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Shingles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Shingles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic recurrent multifocal osteomyelitis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic recurrent multifocal osteomyelitis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyper IgE recurrent infection syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic recurrent multifocal osteomyelitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic recurrent multifocal osteomyelitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent hypersomnia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Epithelial recurrent erosion dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial recurrent erosion dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent axon collateral Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Recurrent fever Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent subcortical infarcts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent subcortical infarcts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyper-IgE recurrent infection syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyper-IgE recurrent infection syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Epithelial recurrent erosion dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Epithelial recurrent erosion dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent pancreatitis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent infections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute Recurrent Myoglobinuria Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute Recurrent Myoglobinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent respiratory infections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent respiratory infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent Neisseria infections due to factor D deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent Neisseria infections due to factor D deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Otitis media (recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Otitis media (chronic/recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (chronic/recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
X-linked severe combined immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, early-onset, severe Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency 18, severe combined immunodeficiency variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency 18, severe combined immunodeficiency variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperparathyroidism, neonatal severe Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperparathyroidism, neonatal severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia 3, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom 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. |
Severe X-linked myotubular myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia 6, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency, atypical Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency, atypical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia 2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe congenital neutropenia 4, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe myoclonic epilepsy in infancy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, early-onset severe Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, severe, due to leptin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sialic acid storage disease, severe infantile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Hyperparathyroidism, Neonatal Severe Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency from the curated CTD Gene-Disease Associations dataset. |
Severe Dengue Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Dengue from the curated CTD Gene-Disease Associations dataset. |
Abnormalities, Severe Teratoid Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abnormalities, Severe Teratoid from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency due to adenosine deaminase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset. |
Severe Acute Respiratory Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Acute Respiratory Syndrome from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset. |
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset. |
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency with sensitivity to ionizing radiation from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Severe Congenital, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Polycystic kidneys, severe infantile with tuberous sclerosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Severe Congenital, Autosomal Recessive 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Severe Congenital, Autosomal Recessive 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset. |
severe combined immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease severe combined immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
severe congenital neutropenia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease severe congenital neutropenia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
severe acute respiratory syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe acute respiratory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe congenital neutropenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe nonproliferative diabetic retinopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe nonproliferative diabetic retinopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe combined immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe combined immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe pre-eclampsia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe type iii hyperlipoproteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe type iii hyperlipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyper-ige syndrome and severe eczema. atopy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyper-ige syndrome and severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe trauma. mortality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe trauma. mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe childhood thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sars (severe acute respiratory syndrome) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sars (severe acute respiratory syndrome) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyper-ige syndrome. severe eczema. atopy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyper-ige syndrome. severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe desmoid phenotype Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe desmoid phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mild and severe substance abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mild and severe substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe malaria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
communicable diseases; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease communicable diseases; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe acute radiotherapy side effects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe acute radiotherapy side effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe hyperkinetic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe hyperkinetic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe sepsis in blunt trauma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe sepsis in blunt trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphopenia; scid; severe combined immunodeficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphopenia; scid; severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe ulcerative colitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe ulcerative colitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; osteonecrosis; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; osteonecrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe chronic neutropenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe chronic neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
x-linked severe combined immunodeficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease x-linked severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe rsv bronchiolitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe rsv bronchiolitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
outcome after severe injury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease outcome after severe injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe sepsis after trauma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe sepsis after trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
immunologic deficiency syndromes; severe combined immunodeficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease immunologic deficiency syndromes; severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe photoaging of facial skin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term severe in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
SCID - Severe combined immunodeficiency_Lung Tissue_GSE3414 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during SCID - Severe combined immunodeficiency_Lung Tissue_GSE3414 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Treatment response for severe sepsis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Treatment response for severe sepsis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Acne (severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Acne (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease (severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Myopia (severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Myopia (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease (moderate to severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma (childhood, severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
severe osteoporosis Gene SetFrom HPO Gene-Disease Associations genes associated with the severe osteoporosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe platyspondyly Gene SetFrom HPO Gene-Disease Associations genes associated with the severe platyspondyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe photosensitivity Gene SetFrom HPO Gene-Disease Associations genes associated with the severe photosensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe hydrops fetalis Gene SetFrom HPO Gene-Disease Associations genes associated with the severe hydrops fetalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe carpal ossification delay Gene SetFrom HPO Gene-Disease Associations genes associated with the severe carpal ossification delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe lactic acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the severe lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe t-cell immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the severe t-cell immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe combined immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the severe combined immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe visual impairment Gene SetFrom 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. |
intellectual disability, severe Gene SetFrom HPO Gene-Disease Associations genes associated with the intellectual disability, severe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the severe hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe failure to thrive Gene SetFrom HPO Gene-Disease Associations genes associated with the severe failure to thrive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe b lymphocytopenia Gene SetFrom HPO Gene-Disease Associations genes associated with the severe b lymphocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe intrauterine growth retardation Gene SetFrom HPO Gene-Disease Associations genes associated with the severe intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe short-limb dwarfism Gene SetFrom HPO Gene-Disease Associations genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the severe hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe muscular hypotonia Gene SetFrom HPO Gene-Disease Associations genes associated with the severe muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe demyelination of the white matter Gene SetFrom HPO Gene-Disease Associations genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe sensorineural hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the severe sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe t lymphocytopenia Gene SetFrom HPO Gene-Disease Associations genes associated with the severe t lymphocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe myopia Gene SetFrom HPO Gene-Disease Associations genes associated with the severe myopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe limb shortening Gene SetFrom HPO Gene-Disease Associations genes associated with the severe limb shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the severe short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe periodontitis Gene SetFrom HPO Gene-Disease Associations genes associated with the severe periodontitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe postnatal growth retardation Gene SetFrom HPO Gene-Disease Associations genes associated with the severe postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe global developmental delay Gene SetFrom HPO Gene-Disease Associations genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Severe Acute Respiratory Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Severe Acute Respiratory Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Severe Combined Immunodeficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Severe Combined Immunodeficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
mental retardation, severe, with spasticity and tapetoretinal degeneration Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency due to il2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
retinal dystrophy, early-onset severe Gene SetFrom OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset. |
ulna and fibula, absence of, with severe limb deficiency Gene SetFrom 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. |
insulin resistance, severe, digenic Gene SetFrom OMIM Gene-Disease Associations genes associated with the insulin resistance, severe, digenic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital 1, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
{obesity, severe, susceptibility to, bmiq9} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {obesity, severe, susceptibility to, bmiq9} phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital 3, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency, t cell-negative, b-cell/natural killer-cell positive Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency, t cell-negative, b-cell/natural killer-cell positive phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency due to ada deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital, 6, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital, 6, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
encephalopathy, neonatal severe Gene SetFrom OMIM Gene-Disease Associations genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset. |
{obesity, severe, and type ii diabetes} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {obesity, severe, and type ii diabetes} phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital, 5, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, severe Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, severe phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset. |
{influenza, severe, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {influenza, severe, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency, b cell-negative Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency, b cell-negative phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency, athabascan type Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency, athabascan type phenotype from the curated OMIM Gene-Disease Associations dataset. |
polycystic kidney disease, infantile severe, with tuberous sclerosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital 4, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 4, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary disease, chronic obstructive, severe early-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom OMIM Gene-Disease Associations genes associated with the alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency, t-cell negative, b-cell/natural killer cell-positive type Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency, t-cell negative, b-cell/natural killer cell-positive type phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malaria, severe, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malaria, severe, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malaria, severe, resistance to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malaria, severe, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, reducing body, x-linked, severe early-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutropenia, severe congenital 2, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
Severe Acute Respiratory Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Acute Respiratory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Visual Impairment Gene SetFrom 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. |
Mental Disorders, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mental Disorders, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Combined Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Hypoglycaemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hypoglycaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Intellectual Disability Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Epstein Barr Virus Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Epstein Barr Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Sepsis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Sensorineural Hearing Impairment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Myopia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infantile Severe Myoclonic Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infantile Severe Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Dementia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Hypoxic Ischemic Encephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Dengue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Dengue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Chronic Obstructive Pulmonary Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Chronic Obstructive Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autism, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autism, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Acute Malnutrition Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Acute Malnutrition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Aplastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Intellectual Disability And Progressive Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability And Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Congenital Microcephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Congenital Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Expressive Language Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucopolysaccharidosis, Type Vi, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucopolysaccharidosis, Type Vi, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Malnutrition Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Malnutrition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Nonproliferative Diabetic Retinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Nonproliferative Diabetic Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Alpha Thalassemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Fever With Thrombocytopenia Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Fever With Thrombocytopenia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Alcohol Dependence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Alcohol Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Bronchopulmonary Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Bronchopulmonary Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Persistent Asthma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Acute Respiratory Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Acute Respiratory Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Asthma With Fungal Sensitisation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Asthma With Fungal Sensitisation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Generalized Recessive Dystrophic Epidermolysis Bullosa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Generalized Recessive Dystrophic Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Severe Refractory Exacerbation Of Asthma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Severe Refractory Exacerbation Of Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Granulocytopenia Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Granulocytopenia Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Beta Thalassemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Beta Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Pediatric Obstructive Sleep Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Pediatric Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Athabaskan Severe Combined Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Athabaskan Severe Combined Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe [Duchenne] Muscular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe [Duchenne] Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Receptive Language Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Receptive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reaction To Severe Stress, And Adjustment Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reaction To Severe Stress, And Adjustment Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Copd, Severe Early-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copd, Severe Early-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Short-Limb Dwarfism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Short-Limb Dwarfism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe T-Cell Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe T-Cell Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Galactose Epimerase Deficiency, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Galactose Epimerase Deficiency, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Greig Cephalopolysyndactyly Syndrome, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Greig Cephalopolysyndactyly Syndrome, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Dehydration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Dehydration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Left Ventricular Systolic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Costello Syndrome, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Costello Syndrome, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hunter'S Syndrome, Severe Form Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hunter'S Syndrome, Severe Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth Restriction, Severe, With Distinctive Facies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth Restriction, Severe, With Distinctive Facies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Opioid Use Disorder, Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Opioid Use Disorder, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alpha/Beta T-Cell Lymphopenia With Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alpha/Beta T-Cell Lymphopenia With Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Early Childhood Onset Retinal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Laryngospasm, Severe Neonatal Episodic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Laryngospasm, Severe Neonatal Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Global Developmental Delay Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Muscular Hypotonia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Diarrhea Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe B Lymphocytopenia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe B Lymphocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Psychomotor Retardation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Dry Skin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Dry Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Congenital Neutropenia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Congenital Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Cutaneous Adverse Reactions (Smq) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Cutaneous Adverse Reactions (Smq) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early Severe Fetal Akinesia Sequence Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Severe Fetal Akinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Postnatal Growth Retardation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Failure To Thrive Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Failure To Thrive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Photosensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Photosensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Intrauterine Growth Retardation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Generalized Osteoporosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Generalized Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Limb Shortening Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Limb Shortening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Platyspondyly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Platyspondyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Headache Severe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Headache Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Lactic Acidosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Speech Delay Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Speech Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Hydrocephalus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Influenza, Severe, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Influenza, Severe, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Demyelination Of The White Matter Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Demyelination Of The White Matter in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Hydrops Fetalis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Hydrops Fetalis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Gastroesophageal Reflux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Gastroesophageal Reflux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Feeding Problems Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Feeding Problems in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Carpal Ossification Delay Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Carpal Ossification Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe congenital neutropenia type 4 (G6PC3) Gene Setproteins participating in the Severe congenital neutropenia type 4 (G6PC3) pathway from the Reactome Pathways 2024 dataset. |
Severe combined immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe combined immunodeficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Severe congenital neutropenia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital neutropenia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
X-linked severe combined immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked severe combined immunodeficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Severe combined immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe combined immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe COVID-19 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe COVID-19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe acute respiratory syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe acute respiratory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked severe combined immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked severe combined immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe pre-eclampsia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual disability-severe speech delay-mild dysmorphism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
non-severe COVID-19 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-severe COVID-19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
adult-onset severe asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease adult-onset severe asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe combined immunodeficiency with sensitivity to ionizing radiation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked severe congenital neutropenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe nonproliferative diabetic retinopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe nonproliferative diabetic retinopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant severe congenital neutropenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Persistent severe asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent severe asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital neutropenia 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital neutropenia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Susceptibility to severe coronavirus disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Susceptibility to severe coronavirus disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early onset and severe retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset and severe retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe neurodegenerative syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neurodegenerative syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to DCLRE1C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to DCLRE1C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Athabaskan severe combined immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Athabaskan severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-childhood-onset retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe global developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe X-linked myotubular myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe intellectual deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neonatal severe primary hyperparathyroidism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal severe primary hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
T-B+ severe combined immunodeficiency due to JAK3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the T-B+ severe combined immunodeficiency due to JAK3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked severe combined immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked severe congenital neutropenia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe neonatal-onset encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe myoclonic epilepsy in infancy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ZAP70-Related Severe Combined Immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ZAP70-Related Severe Combined Immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe achondroplasia-developmental delay-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe sensorineural hearing impairment Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-severe speech delay-mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe intellectual disability-progressive spastic diplegia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-progressive spastic diplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CARD11 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CARD11 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe congenital neutropenia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe X-linked mitochondrial encephalomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe X-linked mitochondrial encephalomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CTPS1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CTPS1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe underweight in infancy childhood and adolescence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe underweight in infancy childhood and adolescence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to CSF3R deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe neurodevelopmental delay Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neurodevelopmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CARMIL2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CARMIL2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Susceptibility to severe COVID- Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Susceptibility to severe COVID- phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intermediate severe Salla disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Intermediate severe Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to DNA-PKcs deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to DNA-PKcs deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CORO1A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CORO1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to IKK2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to IKK2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe dermatitis-multiple allergies-metabolic wasting syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe dermatitis-multiple allergies-metabolic wasting syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to LCK deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to LCK deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |