Severe Depression

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Results for "Severe Depression": 552 gene sets

Name
Severe Depression Gene Set From 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 Major Depression With Psychotic Features Gene Set From 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.
Severe Recurrent Major Depression Gene Set From 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.
Frontonasal Dysplasia, Severe Microphthalmia, Severe Facial Clefting Syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
major mood disorders: bipolar, major depression Gene Set From 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.
schizophrenia ; depression Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
neuroticism, major depression, and anxiety disorders Gene Set From 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.
lipid levels; depression Gene Set From 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 Set From 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.
major depression Gene Set From 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.
depression and response to antidepressant treatment Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From GWASdb SNP-Phenotype Associations genes associated with the depression phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
depression Gene Set From 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 Set From 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 Set From KEGG Pathways proteins participating in the long term depression pathway from the KEGG Pathways dataset.
absent long term depression Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the {unipolar depression, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
depression Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Recurrent Depression Gene Set From 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.
Endogenous Depression Gene Set From 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.
Major Depression, Single Episode Gene Set From 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.
Clinical Depression Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Major depression and alcohol dependence Gene Set From 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 Set From 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.
Depression in multiple sclerosis (pre-diagnosis) Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Nicotine dependence and major depression (severity of comorbidity) Gene Set From 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 Set From 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.
Seasonality and depression Gene Set From 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 Set From 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 Set From 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 Set From 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 major depressive disorder (self-reported) Gene Set From 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.
Broad depression or major depressive disorder (recurrent) Gene Set From 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.
Broad depression or bipolar disorder Gene Set From 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 Set From 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.
Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene Set From 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.
Treatment resistant depression Gene Set From 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.
Response to ketamine in bipolar disorder or major depression (antidepressant effects) Gene Set From 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 Set From 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.
Depression x maternal smoking during pregnancy interaction Gene Set From 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 Set From KEGG Pathways 2026 proteins participating in the Long-term depression pathway from the KEGG Pathways 2026 dataset.
X-linked severe combined immunodeficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe X-linked myotubular myopathy Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe myoclonic epilepsy in infancy Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency from the curated CTD Gene-Disease Associations dataset.
Severe Dengue Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Dengue from the curated CTD Gene-Disease Associations dataset.
Abnormalities, Severe Teratoid Gene Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 recurrent varicella Gene Set From 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.
severe visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, severe Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
insulin resistance, severe, digenic Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Disorders, Severe Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Varicella, Severe Recurrent Gene Set From 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.
Athabaskan Severe Combined Immunodeficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngospasm, Severe Neonatal Episodic Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Reactome Pathways 2024 proteins participating in the Severe congenital neutropenia type 4 (G6PC3) pathway from the Reactome Pathways 2024 dataset.
Severe combined immunodeficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset and severe retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe neurodegenerative syndrome Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe global developmental delay Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe muscular hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe muscular hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to LAT deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to LAT deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the CV-A6-associated hand, foot, and mouth disease (severe vs mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe COVID-19 infection with respiratory failure (analysis I) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe COVID-19 infection with respiratory failure (analysis I) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe COVID-19 infection with respiratory failure (analysis II) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe COVID-19 infection with respiratory failure (analysis II) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Statin-induced myopathy (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pelvic organ prolapse (moderate/severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pelvic organ prolapse (moderate/severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe influenza A (H1N1) infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe influenza A (H1N1) infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe malaria Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe malaria phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe malaria (adjusted for sickle cell variant rs334) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe malaria (adjusted for sickle cell variant rs334) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe aplastic anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aplastic anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe aortic features in Marfan syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aortic features in Marfan syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe skin toxicity response to cetuximab in colorectal cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe skin toxicity response to cetuximab in colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (moderate or severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (moderate or severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acne (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acne (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis (hand, severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis (hand, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Myopia (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Myopia (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of antiepileptic drugs in severe mental disorder (concentration drug ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of antiepileptic drugs in severe mental disorder (concentration drug ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of antipsychotic drugs in severe mental disorder (concentration drug ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of antipsychotic drugs in severe mental disorder (concentration drug ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pharmacokinetics of olanzapine in severe mental disorder (concentration dose ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pharmacokinetics of olanzapine in severe mental disorder (concentration dose ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe mucosal involvement Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe mucosal involvement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe diabetic retinopathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe diabetic retinopathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypospadias (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypospadias (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Glucosuria (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glucosuria (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hematuria (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hematuria (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proteinuria (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proteinuria (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ketonuria (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ketonuria (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Treatment response for severe sepsis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Treatment response for severe sepsis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to mepolizumab in severe asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to mepolizumab in severe asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced severe leukopenia in inflammatory bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced severe leukopenia in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced acute severe leukopenia in inflammatory bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced acute severe leukopenia in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced severe alopecia in inflammatory bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced severe alopecia in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erosive tooth wear (severe vs none or mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erosive tooth wear (severe vs none or mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe progression in rheumatoid arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe progression in rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe bacterial meningitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe bacterial meningitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe exacerbations in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Moderate or severe diarrhoea in darapladib-treated cardiovascular disease (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Moderate or severe diarrhoea in darapladib-treated cardiovascular disease (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe gingival inflammation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe gingival inflammation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe gastric atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe gastric atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe insulin-deficient type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe insulin-deficient type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe insulin-resistant type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe insulin-resistant type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe autoimmune type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe autoimmune type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Symptoms in placebo-treated COVID-19 outpatients at risk of severe disease (time to remission) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Symptoms in placebo-treated COVID-19 outpatients at risk of severe disease (time to remission) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe coronary stenosis (young age of onset interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe coronary stenosis (young age of onset interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Severe Depression Gene Set

Severe Major Depression With Psychotic Features Gene Set

Severe Recurrent Major Depression Gene Set

Frontonasal Dysplasia, Severe Microphthalmia, Severe Facial Clefting Syndrome Gene Set

Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome Gene Set

Erosive tooth wear (severe vs non-severe) Gene Set

Depression Gene Set

mental depression Gene Set

mental depression Gene Set

endogenous depression Gene Set

repiratory depression Gene Set

myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set

schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior Gene Set

major mood disorders: bipolar, major depression Gene Set

schizophrenia ; depression Gene Set

parkinson's disease; depression Gene Set

anxiety and hostility and depression Gene Set

depression Gene Set

depression, psychosis and antipsychotic response Gene Set

schizophrenia; manic depression Gene Set

suicide; depression Gene Set

depression; alcohol withdrawal Gene Set

alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior Gene Set

obesity; depression; cerebrovascular disease Gene Set

depression ; personality Gene Set

depression ; metabolic syndrome Gene Set

myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; Gene Set

anxiety disorder; alcoholism; depression; narcolepsy Gene Set

schizophrenia ; depression ; bipolar disorder Gene Set

anxiety disorder; depression Gene Set

depression in parkinson's disease Gene Set

neuroticism, major depression, and anxiety disorders Gene Set

lipid levels; depression Gene Set

depression; neuroticism Gene Set

major depression Gene Set

depression and response to antidepressant treatment Gene Set

depressed suicide; suicide due to depression Gene Set

alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set

depression, postpartum Gene Set

depression, postpartum; Gene Set

bipolar disorder; depression Gene Set

depression; treatment with fluoxetine Gene Set

depression, postpartum; pregnancy complications Gene Set

depression; thrombocyte mao activity Gene Set

aura anxiety and depression Gene Set

depression ; long qt syndrome Gene Set

depression ; bipolar disorder Gene Set

depression Gene Set

regulation of long term synaptic depression Gene Set

long term synaptic depression Gene Set

negative regulation of long term synaptic depression Gene Set

Depression and alcohol dependence Gene Set

Schizophrenia, bipolar disorder and depression (combined) Gene Set

Suicidal ideation in depression or bipolar disorder Gene Set

Depression (quantitative trait) Gene Set

Suicide attempts in depression or bipolar disorder Gene Set

mental depression Gene Set

endogenous depression Gene Set

depression Gene Set

depression Gene Set

Depression, Postpartum Gene Set

long term depression Gene Set

absent long term depression Gene Set

decreased synaptic depression Gene Set

increased synaptic depression Gene Set

reduced long term depression Gene Set

abnormal depression-related behavior Gene Set

abnormal synaptic depression Gene Set

abnormal long term depression Gene Set

{unipolar depression, susceptibility to} Gene Set

depression Gene Set

Depression Gene Set

Mental Depression Gene Set

Unipolar Depression Gene Set

Central Nervous System Depression (Disorder) Gene Set

Post Stroke Depression Gene Set

Recurrent Depression Gene Set

Endogenous Depression Gene Set

Major Depression, Single Episode Gene Set