familial encephalopathy with neuroserpin inclusion bodies

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Results for "familial encephalopathy with neuroserpin inclusion bodies": 54 genes, 1005 gene sets

Name
ETHE1 Gene ethylmalonic encephalopathy* 1* This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]
SERPINI1 Gene serpin peptidase inhibitor, clade I (neuroserpin), member 1 This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
AAA1 Gene aortic aneurysm, familial* abdominal 1*
AAA3 Gene Aneurysm, familial* abdominal 3*
AAA2 Gene Aortic aneurysm, familial* abdominal 2*
AAA4 Gene Aortic aneurysm, familial* abdominal, 4*
ETL6 Gene Epilepsy, familial* temporal lobe, 6*
RCM2 Gene cardiomyopathy, familial* restrictive, 2*
ATFB8 Gene Atrial fibrillation, familial, 8
HNFJ3 Gene Hyperuricemic nephropathy, familial* juvenile, 3*
GPSC Gene gliosis, familial* progressive subcortical*
BHD Gene Beukes familial* hip dysplasia*
FAME4 Gene Epilepsy, familial* adult myoclonic, 4*
FAME3 Gene Epilepsy, familial* adult myoclonic, 3*
PFHB2 Gene Progressive familial* heart block, type II*
BFIS1 Gene benign familial* infantile convulsions*
HBN1 Gene Progressive familial* heart block, type I, locus 1*
ETL2 Gene epilepsy, familial* temporal lobe*
FHII Gene Hyperaldosteronism, familial, type II
FCMTE2 Gene familial cortical myoclonic tremor with epilepsy 2
FCMTE1 Gene familial cortical myoclonic tremor with epilepsy 1
GLM4 Gene Glioma, familial, 1
PSHK2 Gene Pseudohyperkalemia, familial, 2, due to red cell leak
VVS Gene Syncope, familial* vasovagal*
BFIS4 Gene Convulsions, benign familial* infantile, 4*
ATFB1 Gene Atrial fibrillation, familial* 1*
ATFB2 Gene familial atrial fibrillation 2
SXI2 Gene X inactivation, familial* skewed, 2*
BFIC2 Gene Benign familial* infantile convulsions-2*
FMTLE Gene Epilepsy, familial* mesial temporal lobe*
STUT3 Gene Stuttering, familial* persistent, 3*
STUT2 Gene Stuttering, familial* persistent 2*
STUT1 Gene Stuttering, familial* persistent 1*
STUT4 Gene Stuttering, familial* persistent, 4*
BRCD1 Gene cancer, familial, with* in vitro radioresistance*
MGR2 Gene Migraine, familial* typical, susceptibility to*
MGR3 Gene Migraine, familial, with* or without aura, susceptibility to*
MFT2 Gene Trichoepithelioma, multiple familial, 2
FEB9 Gene Febrile convulsions, familial, 9
ATFB5 Gene Atrial fibrillation, familial, 5
HTGS Gene Hypertriglyceridemia, familial
DIP Gene interstitial pneumonitis, desquamative, familial
CMH21 Gene Cardiomyopathy, familial* hypertrophic, 21*
CANDF1 Gene candidiasis, familial* 1*
ATPLS Gene antiphospholipid syndrome, familial
EOS Gene eosinophilia, familial
FEB10 Gene Febrile convulsions, familial, 10
LVNC2 Gene noncompaction of left ventricular myocardium, familial* isolated, autosomal dominant 2*
THCYTX Gene Thrombocytosis, familial* X-linked*
CMS1A1 Gene myasthenia gravis, familial* infantile, 1*
BPPV Gene vestibulopathy, familial
AAT2 Gene Aortic aneurysm, familial* thoracic 2*
AAT1 Gene Aortic aneurysm, familial* thoracic 1*
NKCD Gene Natural killer cell deficiency, familial* isolated*
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Familial Encephalopathy With Neuroserpin Inclusion Bodies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Encephalopathy With Neuroserpin Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial encephalopathy with neuroserpin inclusion bodies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial encephalopathy with neuroserpin inclusion bodies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
muscle fiber inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neutrophil inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the neutrophil inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber cytoplasmatic inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber cytoplasmatic inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
foam cells with lamellar inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the foam cells with lamellar inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the cerebral inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Muscle Fiber Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fiber Cytoplasmatic Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Cytoplasmatic Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ubiquitin-Positive Cerebral Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ubiquitin-Positive Cerebral Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leukocyte Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leukocyte Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neutrophil Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neutrophil Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foam Cells With Lamellar Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foam Cells With Lamellar Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
nervous system inclusion bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nervous system inclusion bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Neutrophil inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutrophil inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
neuroserpin Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neuroserpin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Familial Acute Necrotizing Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Necrotizing Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial acute necrotizing encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial acute necrotizing encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Ketone Bodies Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Ketone Bodies from the curated CTD Gene-Chemical Interactions dataset.
bodies Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term bodies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
HOXB4_induction_GDS3036_138_mouse_ES cell-derived embryoid bodies (EBs) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the HOXB4_induction_GDS3036_138_mouse_ES cell-derived embryoid bodies (EBs) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
gemini of coiled bodies Gene Set From GO Cellular Component Annotations 2015 proteins localized to the gemini of coiled bodies cellular component from the curated GO Cellular Component Annotations 2015 dataset.
absent or minimally ossified vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the absent or minimally ossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nemaline bodies Gene Set From HPO Gene-Disease Associations genes associated with the nemaline bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cuboid-shaped vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the cuboid-shaped vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior clefting of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the anterior clefting of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
biconcave vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the biconcave vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small cervical vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the small cervical vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
beaking of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the beaking of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tall lumbar vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the tall lumbar vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
beaking of vertebral bodies t12-l3 Gene Set From HPO Gene-Disease Associations genes associated with the beaking of vertebral bodies t12-l3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sandwich appearance of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the sandwich appearance of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal form of the vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior scalloping of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the posterior scalloping of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior wedging of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the posterior wedging of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplastic vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the hypoplastic vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent in utero ossification of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disc-like vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the disc-like vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unossified vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the unossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior rounding of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the anterior rounding of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ovoid vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the ovoid vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lewy bodies Gene Set From HPO Gene-Disease Associations genes associated with the lewy bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
synthesis and degradation of ketone bodies Gene Set From KEGG Pathways proteins participating in the synthesis and degradation of ketone bodies pathway from the KEGG Pathways dataset.
small alveolar lamellar bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent alveolar lamellar bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pml bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pml bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of howell-jolly bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of howell-jolly bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fusion of vertebral bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enlarged alveolar lamellar bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of heinz bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of heinz bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bodies Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term bodies in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Synthesis of Ketone Bodies Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Ketone Bodies pathway from the Reactome Pathways dataset.
Utilization of Ketone Bodies Gene Set From Reactome Pathways 2014 proteins participating in the Utilization of Ketone Bodies pathway from the Reactome Pathways dataset.
Synthesis and Degradation of Ketone Bodies(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Synthesis and Degradation of Ketone Bodies(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Synthesis and Degradation of Ketone Bodies(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Synthesis and Degradation of Ketone Bodies(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Howell-Jolly Bodies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Howell-Jolly Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cuboid-Shaped Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cuboid-Shaped Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ovoid Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ovoid Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Form Of The Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Form Of The Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nemaline Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nemaline Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Cervical Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Cervical Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Beaking Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beaking Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Biconcave Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biconcave Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unossified Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unossified Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent In Utero Ossification Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent In Utero Ossification Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Or Minimally Ossified Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Or Minimally Ossified Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anterior Clefting Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Clefting Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sandwich Appearance Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sandwich Appearance Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Irregularity Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregularity Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disc-Like Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disc-Like Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Scalloping Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Scalloping Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tall Lumbar Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tall Lumbar Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Wedging Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Wedging Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anterior Rounding Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Rounding Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Biconvex Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biconvex Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
increased number of pulmonary neuroendocrine bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fusion of vertebral bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged alveolar lamellar bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased number of Heinz bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased number of Heinz bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased number of Howell-Jolly bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased number of Howell-Jolly bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small alveolar lamellar bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
persistent ultimobranchial bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the persistent ultimobranchial bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent alveolar lamellar bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Lafora bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Lafora bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent pulmonary neuroendocrine bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent pulmonary neuroendocrine bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal PML bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal PML bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased number of pulmonary neuroendocrine bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Mallory bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Mallory bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Lewy bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Lewy bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Synthesis of Ketone Bodies Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of Ketone Bodies pathway from the Reactome Pathways 2024 dataset.
Utilization of Ketone Bodies Gene Set From Reactome Pathways 2024 proteins participating in the Utilization of Ketone Bodies pathway from the Reactome Pathways 2024 dataset.
Gemini of coiled bodies Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Gemini of coiled bodies cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Gemini of coiled bodies Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Gemini of coiled bodies cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dementia with Lewy bodies Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dementia with Lewy bodies phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Inclusion body myopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beta-thalassemia, dominant inclusion body type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
nuclear inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores proteins localized to the inclusion body cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
nuclear inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lewy body-like hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
fibrillary inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
skein-like inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
glial cytoplasmic inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta Thalassemia, Dominant Inclusion Body Type from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy 3, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Microvillus inclusion disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microvillus inclusion disease from the curated CTD Gene-Disease Associations dataset.
Inclusion body myopathy autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion body myopathy autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Myositis, Inclusion Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myositis, Inclusion Body from the curated CTD Gene-Disease Associations dataset.
inclusion conjunctivitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
inclusion body myositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inclusion body myositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myositis, sporadic inclusion-body Gene Set From GAD Gene-Disease Associations genes associated with the disease myositis, sporadic inclusion-body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
distal myopathies; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sporadic inclusion body myositis Gene Set From GAD Gene-Disease Associations genes associated with the disease sporadic inclusion body myositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deglutition disorders; muscle weakness; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease deglutition disorders; muscle weakness; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inclusion Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term inclusion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Inclusion Body Myositides_Muscle tissue_GSE3112 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Inclusion Body Myositides_Muscle tissue_GSE3112 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
inclusion body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the inclusion body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Myositis, Inclusion Body Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myositis, Inclusion Body phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
alpha-synuclein inclusion body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the alpha-synuclein inclusion body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thalassemia-beta, dominant inclusion-body Gene Set From OMIM Gene-Disease Associations genes associated with the thalassemia-beta, dominant inclusion-body phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
microvillus inclusion disease Gene Set From OMIM Gene-Disease Associations genes associated with the microvillus inclusion disease phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
sporadic inclusion-body myositis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease sporadic inclusion-body myositis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Inclusion Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microvillus Inclusion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microvillus Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inclusion Body Myositis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myositis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Inclusion-Body Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Inclusion-Body Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Intranuclear Inclusion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Intranuclear Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Inclusion Cyst Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Inclusion Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Beta Thalassemia, Dominant Inclusion Body Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Germinal Inclusion Cyst Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Germinal Inclusion Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inclusion Body Myopathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2023 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2023 dataset.
glial cytoplasmic inclusion Gene Set From GO Cellular Component Annotations 2023 proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2023 dataset.
alpha-synuclein inclusion body Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alpha-synuclein inclusion body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Inclusion body myositis Gene Set From WikiPathways Pathways 2024 proteins participating in the Inclusion body myositis pathway from the WikiPathways Pathways 2024 dataset.
Calcium mediated T cell apoptosis involved in inclusion body myositis Gene Set From WikiPathways Pathways 2024 proteins participating in the Calcium mediated T cell apoptosis involved in inclusion body myositis pathway from the WikiPathways Pathways 2024 dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2025 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2025 dataset.
glial cytoplasmic inclusion Gene Set From GO Cellular Component Annotations 2025 proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Microvillus inclusion disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Microvillus inclusion disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Inclusion body myositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Microvillus inclusion disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microvillus inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion conjunctivitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal intranuclear inclusion disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal intranuclear inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nuclear inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Glial cytoplasmic inclusion Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Glial cytoplasmic inclusion cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 proteins localized to the Inclusion body cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Glial cytoplasmic inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
skein-like inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Lewy body-like hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Nuclear inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Fibrillary inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Inclusion body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion-body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion-body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy and brain white matter abnormalities Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy and brain white matter abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early myoclonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
epileptic encephalopathy, early infanitle, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the epileptic encephalopathy, early infanitle, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ethylmalonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ethylmalonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic Encephalopathy, Early Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.
Hypertensive Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertensive Encephalopathy from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Encephalopathy from the curated CTD Gene-Disease Associations dataset.
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Epileptic encephalopathy, Lennox-Gastaut type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic encephalopathy, Lennox-Gastaut type from the curated CTD Gene-Disease Associations dataset.
Wernicke Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wernicke Encephalopathy from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.
Mitochondrial neurogastrointestinal encephalopathy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial neurogastrointestinal encephalopathy syndrome from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 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.
Epileptic Encephalopathy, Early Infantile, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.
Spongiform Encephalopathy with Neuropsychiatric Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spongiform Encephalopathy with Neuropsychiatric Features from the curated CTD Gene-Disease Associations dataset.
Ethylmalonic encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ethylmalonic encephalopathy from the curated CTD Gene-Disease Associations dataset.
glycine encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycine encephalopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycine encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycine encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hepatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early myoclonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
wernicke encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease wernicke encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
toxic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease toxic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypertensive encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypertensive encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic toxic encephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic toxic encephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatic encephalopathy; liver cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatic encephalopathy; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
encephalopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term encephalopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
hypoglycemic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the hypoglycemic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hepatic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the hepatic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
epileptic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the epileptic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acute encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the acute encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mitochondrial encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the mitochondrial encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acute necrotizing encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the acute necrotizing encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Encephalopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Encephalopathy, Bovine Spongiform Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Encephalopathy, Bovine Spongiform phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
spongiform encephalopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spongiform encephalopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 24 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 25 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 26 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 23 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set From OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
ethylmalonic encephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the ethylmalonic encephalopathy 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.
3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
glycine encephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the glycine encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
?epileptic encephalopathy, early infantile, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective ACY1 causes encephalopathy Gene Set From Reactome Pathways 2014 proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways dataset.
Epileptic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epileptic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ethylmalonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ethylmalonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spongiform Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spongiform Encephalopathy 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.
Hypoxic-Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoxic-Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biotin-Responsive Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biotin-Responsive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
3-Methylglutaconic Aciduria Type Iv With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 3-Methylglutaconic Aciduria Type Iv With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uremic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uremic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arsenic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arsenic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy With Suppression Bursts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy With Suppression Bursts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minimal Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minimal Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Reversible Encephalopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Reversible Encephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Myoclonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Myoclonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Traumatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Traumatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Encephalopathy, Infantile Subacute, Of Leigh in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wernicke Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wernicke Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Static Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Static Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Necrotizing Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Necrotizing Encephalopathy Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transmissible Mink Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transmissible Mink Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mercury Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mercury Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Febrile Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Febrile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Static Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Static Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Neurogastrointestinal Encephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spongiform Encephalopathy With Neuropsychiatric Features Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spongiform Encephalopathy With Neuropsychiatric Features in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scn8A-Related Epilepsy With Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scn8A-Related Epilepsy With Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infanctile Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infanctile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycine Encephalopathy With Normal Serum Glycine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycine Encephalopathy With Normal Serum Glycine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infanctile Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infanctile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Epileptic Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Epileptic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
spongiform encephalopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spongiform encephalopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
encephalopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the encephalopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Ethylmalonic encephalopathy Gene Set From WikiPathways Pathways 2024 proteins participating in the Ethylmalonic encephalopathy pathway from the WikiPathways Pathways 2024 dataset.
Defective ACY1 causes encephalopathy Gene Set From Reactome Pathways 2024 proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways 2024 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.
Developmental and epileptic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 14 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 13 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycine encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycine encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ethylmalonic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ethylmalonic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 26 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Toxic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Toxic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic traumatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic traumatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ethylmalonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ethylmalonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hepatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early infantile epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early infantile epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 86 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 86 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early myoclonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertensive encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertensive encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Wernicke encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Wernicke encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycine encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycine encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 80 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 80 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 93 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 93 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 53 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 53 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
TANGO2-related metabolic encephalopathy and arrythmias Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease TANGO2-related metabolic encephalopathy and arrythmias in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Encephalopathy due to defective mitochondrial and peroxisomal fission 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 98 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 98 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 31A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 31A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 60 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 60 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 62 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 62 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 103 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 103 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 91 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 91 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.
Developmental and epileptic encephalopathy 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 66 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 66 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 94 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 94 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 6B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 6B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 65 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 65 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 97 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 97 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 102 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 102 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 67 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 67 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 104 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 104 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 106 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 106 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 74 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 74 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 58 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 58 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 90 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 90 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 72 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 72 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 71 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 71 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 100 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 100 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 96 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 96 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 89 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 89 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early myoclonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ethylmalonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ethylmalonic encephalopathy 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.
Glycine encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycine encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spongiform encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongiform encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to GLUT1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to GLUT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocephaly and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocephaly and epileptic encephalopathy 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.
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Genetic developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early Infantile Epileptic Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early Infantile Epileptic Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Undetermined early-onset epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Undetermined early-onset epileptic encephalopathy 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.
Early onset epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic Infantile Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic Infantile Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Unclassified developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Unclassified developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to defective mitochondrial and peroxisomal fission phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BSCL2-related Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BSCL2-related Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epileptic dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epileptic dyskinetic encephalopathy 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.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atypical glycine encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical glycine encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRIM8-related epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRIM8-related epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RYR3-related Epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RYR3-related Epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HCN2 related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HCN2 related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SNAP25-related early-onset developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SNAP25-related early-onset developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalitis/encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalitis/encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SYNGAP1-related encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SYNGAP1-related encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNA3-associated developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNA3-associated developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GABRA4-related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GABRA4-related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial Mediterranean fever Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, hyperphosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemic nephropathy, familial juvenile, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cancer of breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial aortopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital arthropathy-brachydactyly, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial visceral amyloidosis, Ostertag type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia familial British Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
familial hyperinsulinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia familial 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paroxysmal familial ventricular fibrillation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypercholesterolemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hidradenitis suppurativa, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia, familial Danish Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial dysautonomia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial febrile seizures 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial exudative vitreoretinopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial colorectal cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porphyria cutanea tarda Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonus, familial cortical Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Migraine, familial basilar Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholanemia, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypokalemia-hypomagnesemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenia, limb-girdle, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular fibrillation, paroxysmal familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial erythrocytosis, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperlipidemia, familial combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial amyloid polyneuropathy, Iowa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, familial adult myoclonic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial myxoma, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial juvenile gout Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypobetalipoproteinemia, familial, associated with apob32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 3 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, normophosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd8 deficiency, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial atypical mycobacteriosis, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperthyroxinemia, familial dysalbuminemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 5 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial pulmonary capillary hemangiomatosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoalphalipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal hypouricemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoplastic, glomerulocystic kidney Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cold urticaria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Aneurysm, Familial Abdominal 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.
Familial myelofibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset.
Nephronophthisis, familial juvenile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.
Eosinophilia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, familial visceral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.
STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.
Dementia, familial British Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
CD8 Deficiency, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.
Insomnia, Fatal Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset.
Familial dermographism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperthyroidism, Familial Gestational Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Migraine, Familial Hemiplegic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Cancer, Familial, with In Vitro Radioresistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Hypoparathyroidism familial isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hidradenitis suppurativa, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.
Dementia, familial Danish Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.
Familial medullary thyroid carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.
Interstitial Pneumonitis, Desquamative, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.
Cirrhosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Familial Partial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Keratoacanthoma familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.
Familial Wilms tumor 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial antiphospholipid syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Atrial fibrillation, familial 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.
Meningioma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Cold Autoinflammatory Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Adult Myoclonic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.
Prostate cancer, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
Hyperthyroxinemia, Familial Dysalbuminemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial cylindromatosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Hyperaldosteronism, Familial, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Atrial myxoma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Normophosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.
Periodic fever, familial, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.
Familial schizencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.
Neurofibromatosis, Familial Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.
Reticuloendotheliosis, familial, with eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.
MITRAL VALVE PROLAPSE, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Familial dilated cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Thymoma, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.
Familial apoceruloplasmin deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.
HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Amyloid Neuropathies, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.
CANDIDIASIS, FAMILIAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Stuttering, Familial Persistent 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Temporal Lobe, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypertriglyceridemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial combined hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal familial insomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial mediterranean fever Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial nephrotic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial glomangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypercholesterolemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial partial lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial visceral amyloidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal papillary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial or sporadic prostate cancer. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b100. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies; amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset familial alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdomen, acute; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysbetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease (familial) Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set From GAD Gene-Disease Associations genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial premature myocardial infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset of familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b-100 in a chinese man Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; familial mediterranean fever; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial male-limited precocious puberty. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidaemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial early onset psoriasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypobetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypobetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy in a hungarian family. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in a hungarian family. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease familial melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypocalciuric hypercalcemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hyperinsulinism. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hyperinsulinism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial glucocorticoid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease familial glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial partial lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial partial lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial liver adenomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial liver adenomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea; familial mediterranean fever; pain; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertrophic cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; atherosclerosis; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; atherosclerosis; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial exudative vitreoretinopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial exudative vitreoretinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysautonomia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysautonomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial alzheimer's disease associated Gene Set From GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
greenland familial cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial diabetes insipidus Gene Set From GAD Gene-Disease Associations genes associated with the disease familial diabetes insipidus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial erythrocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial erythrocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial bronchiectasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial bronchiectasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial non-ret c cell hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertension of early onset. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; hyper-igd syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; hyper-igd syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term familial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Parkinson's disease (familial) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
familial hypertriglyceridemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial atrial fibrillation Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial predisposition Gene Set From HPO Gene-Disease Associations genes associated with the familial predisposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperlipidemia, Familial Combined phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paralyses, Familial Periodic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paralyses, Familial Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Familial Mediterranean Fever Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Familial Mediterranean Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lipodystrophy, Familial Partial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lipodystrophy, Familial Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloidosis, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysautonomia, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysautonomia, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloid Neuropathies, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloid Neuropathies, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Insomnia, Fatal Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Insomnia, Fatal Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial focal, with variable foci Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, familial primary Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrial fibrillation, familial, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
digital arthropathy-brachydactyly, familial Gene Set From OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial basilar Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 8 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 9 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
insomnia, fatal familial Gene Set From OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dysautonomia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

Harmonizome 3.0

ETHE1 Gene

SERPINI1 Gene

AAA1 Gene

AAA3 Gene

AAA2 Gene

AAA4 Gene

ETL6 Gene

RCM2 Gene

ATFB8 Gene

HNFJ3 Gene

GPSC Gene

BHD Gene

FAME4 Gene

FAME3 Gene

PFHB2 Gene

BFIS1 Gene

HBN1 Gene

ETL2 Gene

FHII Gene

FCMTE2 Gene

FCMTE1 Gene

GLM4 Gene

PSHK2 Gene

VVS Gene

BFIS4 Gene

ATFB1 Gene

ATFB2 Gene

SXI2 Gene

BFIC2 Gene

FMTLE Gene

STUT3 Gene

STUT2 Gene

STUT1 Gene

STUT4 Gene

BRCD1 Gene

MGR2 Gene

MGR3 Gene

MFT2 Gene

FEB9 Gene

ATFB5 Gene

HTGS Gene

DIP Gene

CMH21 Gene

CANDF1 Gene

ATPLS Gene

EOS Gene

FEB10 Gene

LVNC2 Gene

THCYTX Gene

CMS1A1 Gene

BPPV Gene

AAT2 Gene

AAT1 Gene

NKCD Gene

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

Familial Encephalopathy With Neuroserpin Inclusion Bodies Gene Set

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

encephalopathy, familial, with neuroserpin inclusion bodies Gene Set

muscle fiber inclusion bodies Gene Set

neutrophil inclusion bodies Gene Set

muscle fiber cytoplasmatic inclusion bodies Gene Set

foam cells with lamellar inclusion bodies Gene Set

cerebral inclusion bodies Gene Set

Muscle Fiber Inclusion Bodies Gene Set

Muscle Fiber Cytoplasmatic Inclusion Bodies Gene Set

Ubiquitin-Positive Cerebral Inclusion Bodies Gene Set

Leukocyte Inclusion Bodies Gene Set

Neutrophil Inclusion Bodies Gene Set

Foam Cells With Lamellar Inclusion Bodies Gene Set

nervous system inclusion bodies Gene Set

Neutrophil inclusion bodies Gene Set

neuroserpin Gene Set

Familial Acute Necrotizing Encephalopathy Gene Set

Familial encephalopathy Gene Set

Familial acute necrotizing encephalopathy Gene Set

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

amyloidosis, familial; familial mediterranean fever Gene Set