Recurrent Childhood Medulloblastoma

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Results for "Recurrent Childhood Medulloblastoma": 817 gene sets

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Recurrent Childhood Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
childhood medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Childhood Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
recurrent infections in infancy and early childhood Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Recurrent Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Anaplastic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Infections In Infancy And Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
MYC-20876797-MEDULLOBLASTOMA-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the MYC-20876797-MEDULLOBLASTOMA-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Medulloblastoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medulloblastoma from the curated CTD Gene-Disease Associations dataset.
melanotic medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease melanotic medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nodular medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nodular medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
large cell medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease large cell medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adult medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; medulloblastoma Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; medulloblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
medulloblastoma; nijmegen breakage syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease medulloblastoma; nijmegen breakage syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
medulloblastoma Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term medulloblastoma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Mel-18_KD_GDS2724_103_human_DAOY medulloblastoma cells Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Mel-18_KD_GDS2724_103_human_DAOY medulloblastoma cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Bmi-1_KD_GDS2724_102_human_DAOY medulloblastoma cells Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Bmi-1_KD_GDS2724_102_human_DAOY medulloblastoma cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
ALK_KD_GDS2724_105_human_DAOY medulloblastoma cells Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the ALK_KD_GDS2724_105_human_DAOY medulloblastoma cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
OTX2_silencing_GDS4472_136_human_D425 medulloblastoma (MB) cells Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the OTX2_silencing_GDS4472_136_human_D425 medulloblastoma (MB) cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
medulloblastoma Gene Set From HPO Gene-Disease Associations genes associated with the medulloblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Medulloblastoma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Medulloblastoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
increased medulloblastoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased medulloblastoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
medulloblastoma Gene Set From OMIM Gene-Disease Associations genes associated with the medulloblastoma phenotype from the curated OMIM Gene-Disease Associations dataset.
medulloblastoma, desmoplastic Gene Set From OMIM Gene-Disease Associations genes associated with the medulloblastoma, desmoplastic phenotype from the curated OMIM Gene-Disease Associations dataset.
{medulloblastoma} Gene Set From OMIM Gene-Disease Associations genes associated with the {medulloblastoma} phenotype from the curated OMIM Gene-Disease Associations dataset.
medulloblastoma cell Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue medulloblastoma cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
medulloblastoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medulloblastoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medulloblastoma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medulloblastoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Adult Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Melanotic Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Melanotic Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Classic Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Classic Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Cell/Anaplastic Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Large Cell/Anaplastic Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Cell Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Large Cell Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
MYC-20876797-MEDULLOBLASTOMA-HUMAN Gene Set From ChEA Transcription Factor Targets 2022 target genes of the MYC-20876797-MEDULLOBLASTOMA-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
increased medulloblastoma incidence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased medulloblastoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
desmoplastic/nodular medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease desmoplastic/nodular medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Melanotic medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Melanotic medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar vermis medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar vermis medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Large cell medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large cell medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma SHH activated Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma SHH activated in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma SHH activated and TP53 wild-type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma SHH activated and TP53 wild-type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma WNT activated Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma WNT activated in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma non-WNT/non-SHH Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma non-WNT/non-SHH in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma SHH activated and TP53 mutant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medulloblastoma SHH activated and TP53 mutant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brain stem medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brain stem medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medulloblastoma cell Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Medulloblastoma cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Medulloblastoma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medulloblastoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medulloblastoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medulloblastoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medulloblastoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Medulloblastoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Desmoplastic/nodular medulloblastoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Desmoplastic/nodular medulloblastoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoglobinuria, acute recurrent, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hydatidiform mole, recurrent, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hydatidiform mole, recurrent, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
recurrent axon collateral Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset.
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset.
Vertigo, Benign Recurrent, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertigo, Benign Recurrent, 2 from the curated CTD Gene-Disease Associations dataset.
recurrent corneal erosion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
recurrent hypersomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic recurrent miscarriage. Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent bacterial infections Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent bacterial infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory papillomatosis, juvenile-onset; recurrent Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriages Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent cardiovascular event Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent cardiovascular event in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent spontaneous miscarriages Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent abortions Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent abortions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent aphthous stomatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent aphthous stomatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal cord infarction and recurrent venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovary syndrome; pregnancy loss, recurrent Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; in vitro fertilization success Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent spontaneous abortion Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous abortion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent oral ulcers Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent oral ulcers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, late; pregnancy loss, recurrent Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent early fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent deep-vein thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent deep-vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent or chronic idiopathic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent acute pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent acute pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
herpes-associated recurrent lymphocytic meningitis Gene Set From GAD Gene-Disease Associations genes associated with the disease herpes-associated recurrent lymphocytic meningitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent respiratory infections Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent respiratory infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent respiratory papillomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent respiratory papillomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent pregnancy loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term recurrent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
recurrent hypersomnia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease recurrent hypersomnia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
recurrent viral infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent viral infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent mycobacterial infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent infection of the gastrointestinal tract Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent mycobacterium avium complex infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterium avium complex infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent bacterial infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent bacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent aspergillus infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent aspergillus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent abscess formation Gene Set From HPO Gene-Disease Associations genes associated with the recurrent abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent mandibular subluxations Gene Set From HPO Gene-Disease Associations genes associated with the recurrent mandibular subluxations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent fungal infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent staphylococcal infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent staphylococcal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent pharyngitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent pharyngitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bacterial infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent vulvovaginal candidiasis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent vulvovaginal candidiasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bacterial meningitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bacterial meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent pneumonia Gene Set From HPO Gene-Disease Associations genes associated with the recurrent pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent infection of the gastrointestinal tract Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent enteroviral infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent enteroviral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent thrombophlebitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent thrombophlebitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent cerebral hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the recurrent cerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent aspiration pneumonia Gene Set From HPO Gene-Disease Associations genes associated with the recurrent aspiration pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent encephalopathy Gene 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.
recurrent e. coli infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent e. coli infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent mycobacterial infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent mycobacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent aphthous stomatitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent aphthous stomatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent fractures Gene Set From HPO Gene-Disease Associations genes associated with the recurrent fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent pancreatitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent pancreatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent lower respiratory tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent loss of toenails and fingernails Gene Set From HPO Gene-Disease Associations genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe recurrent varicella Gene Set From HPO Gene-Disease Associations genes associated with the severe recurrent varicella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent otitis media Gene Set From HPO Gene-Disease Associations genes associated with the recurrent otitis media phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent meningitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent candida infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent candida infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent urinary tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent urinary tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
failure to thrive secondary to recurrent infections Gene Set From HPO Gene-Disease Associations genes associated with the failure to thrive secondary to recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent cutaneous abscess formation Gene Set From HPO Gene-Disease Associations genes associated with the recurrent cutaneous abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent upper and lower respiratory tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent burkholderia cepacia infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent burkholderia cepacia infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent spontaneous abortion Gene Set From HPO Gene-Disease Associations genes associated with the recurrent spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent sinopulmonary infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent sinopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent klebsiella infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent klebsiella infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent systemic pyogenic infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent systemic pyogenic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent myoglobinuria Gene Set From HPO Gene-Disease Associations genes associated with the recurrent myoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent gram-negative bacterial infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent gram-negative bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent corneal erosions Gene Set From HPO Gene-Disease Associations genes associated with the recurrent corneal erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent infections due to aspiration Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent respiratory infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent respiratory infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spontaneous, recurrent epistaxis Gene Set From HPO Gene-Disease Associations genes associated with the spontaneous, recurrent epistaxis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent singultus Gene Set From HPO Gene-Disease Associations genes associated with the recurrent singultus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent subcortical infarcts Gene Set From HPO Gene-Disease Associations genes associated with the recurrent subcortical infarcts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent skin infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bronchopulmonary infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bronchopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent mycobacterium avium complex infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent mycobacterium avium complex infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent hypoglycemia Gene Set From HPO Gene-Disease Associations genes associated with the recurrent hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent protozoan infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent protozoan infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent upper respiratory tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent meningococcal disease Gene Set From HPO Gene-Disease Associations genes associated with the recurrent meningococcal disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent viral infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent viral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent sinusitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent sinusitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bacterial skin infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bacterial skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent serratia marcescens infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent serratia marcescens infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent streptococcus pneumoniae infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent streptococcus pneumoniae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent neisserial infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent neisserial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent deep vein thrombosis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent deep vein thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent opportunistic infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent opportunistic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bronchitis Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bronchitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent haemophilus influenzae infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent haemophilus influenzae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent cutaneous fungal infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent cutaneous fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent staphylococcus aureus infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent staphylococcus aureus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hydatidiform mole, recurrent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hydatidiform mole, recurrent, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations Gene Set From OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypotrichosis and recurrent skin vesicles Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypotrichosis and recurrent skin vesicles phenotype from the curated OMIM Gene-Disease Associations dataset.
{pregnancy loss, recurrent, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{pregnancy loss, recurrent, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene 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.
hyper-ige recurrent infection syndrome, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
invasive pneumococcal disease, recurrent isolated, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
invasive pneumococcal disease, recurrent isolated, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, recurrent, with pressure palsies Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset.
myoglobinuria, acute recurrent, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
{pregnancy loss, recurrent, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyper-ige recurrent infection syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
vertigo, benign recurrent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vertigo, benign recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Recurrent Otitis Media Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Acute Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Endometrial Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Endometrial Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Ovarian Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Recurrent Intrahepatic Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Aphthous Ulcer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aphthous Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Hepatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Major Depressive Episodes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Major Depressive Episodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Genital Herpes Simplex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Genital Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Sinusitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Upper Respiratory Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Hand Flapping Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hand Flapping in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Hodgkin'S Lymphoma Transformed Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Transformed Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Recurrent Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Herpes Simplex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervix Carcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervix Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Locally Recurrent Malignant Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Locally Recurrent Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Pterygium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pterygium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Brain Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Adult Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Desmoid-Type Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Desmoid-Type Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cerebral Hemorrhage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Optic Neuritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Depressive Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Malignant Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Bronchitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bronchitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Ulcer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colorectal Cancer Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Chronic Lymphoid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Lymphoid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Follicular Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Non-Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Squamous Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Adult Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Hemophagocytic Lymphohistiocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hemophagocytic Lymphohistiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Acute Otitis Media Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Respiratory Papillomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Papillomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oesophageal Carcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngeal Squamous Cell Carcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Squamous Cell Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult T-Cell Lymphoma/Leukaemia Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult T-Cell Lymphoma/Leukaemia Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Large B-Cell Lymphoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lung Adenocarcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lung Adenocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Ovarian Serous Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Serous Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Atypical Teratoid/Rhabdoid Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oropharyngeal Cancer Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oropharyngeal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Rectal Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rectal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Dedifferentiated Liposarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Dedifferentiated Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Cell Lung Cancer Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Cell Lung Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Erosion Of Cornea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Erosion Of Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Recurrent Erosion Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genetic Recurrent Myoglobinuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genetic Recurrent Myoglobinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Bacterial Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Aspiration Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aspiration Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mesothelioma Malignant Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma Malignant Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Pyelonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pyelonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Varicella, Severe Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Varicella, Severe Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Respiratory Tract Infections Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Recurrent Major Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Recurrent Major Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Head And Neck Squamous Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Lung Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Lung Carcinoma Cell Type Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Carcinoma Cell Type Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Cancer Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Head And Neck Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Lung Non-Squamous Non-Small Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Non-Squamous Non-Small Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Infections Due To Aspiration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Due To Aspiration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Larynx Carcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Larynx Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ewing'S Sarcoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ewing'S Sarcoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Infections Of The Middle Ear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Of The Middle Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pregnancy Loss, Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infections, Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infections, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Herpes Simplex Infection Of Eye Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Laryngeal Nerve Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Laryngeal Nerve Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cushing Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cushing Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Subcortical Infarcts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Subcortical Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrahepatic Cholangiocarcinoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholangiocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Mouth Ulcers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Mouth Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Recurrent Pericarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Craniopharyngioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Proliferative Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Proliferative Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Pulmonary Embolism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pulmonary Embolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Systemic Pyogenic Infections Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Systemic Pyogenic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Anaplastic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Malignant Peripheral Nerve Sheath Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Chordoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cystitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cystitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersomnia, Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnia, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Salivary Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
B-Cell Small Lymphocytic Lymphoma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Small Lymphocytic Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Biliary Tract Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Cerebral Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Plasma Cell Myeloma Recurrent Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plasma Cell Myeloma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Salivary Gland Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Gland Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Bacterial Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Thyroid Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Herpes Simplex Labialis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Labialis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Anaplastic Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Respiratory Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Respiratory Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Tumor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Fevers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fevers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spontaneous, Recurrent Epistaxis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous, Recurrent Epistaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Bacterial Infection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Fungal Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fungal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Opportunistic Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Opportunistic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Viral Infection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Mandibular Subluxations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mandibular Subluxations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Skin Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Infection Of The Gastrointestinal Tract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infection Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Upper And Lower Respiratory Tract Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Lower Respiratory Tract Infection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Singultus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Singultus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pregnancy Loss, Recurrent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Spontaneous Abortion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Spontaneous Abortion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Abdominal Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Sinopulmonary Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Sinopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Cutaneous Abscess Formation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Cutaneous Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Enteroviral Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Enteroviral Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Meningococcal Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Meningococcal Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Neisserial Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Neisserial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Failure To Thrive Secondary To Recurrent Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Failure To Thrive Secondary To Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Abscess Formation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Candida Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Candida Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Gastroenteritis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Haemophilus Influenzae Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Haemophilus Influenzae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Streptococcus Pneumoniae Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Streptococcus Pneumoniae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Bronchopulmonary Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Protozoan Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Protozoan Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Staphylococcus Aureus Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcus Aureus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Vulvovaginal Candidiasis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Vulvovaginal Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Myoglobinuria, Recurrent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myoglobinuria, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Encephalopathy Gene 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.
Recurrent Intrapulmonary Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Intrapulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Bacterial Skin Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Headache Recurrent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Headache Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Aspergillus Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Aspergillus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Burkholderia Cepacia Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Burkholderia Cepacia Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Klebsiella Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Klebsiella Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Serratia Marcescens Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Serratia Marcescens Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Mycobacterial Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Paroxysmal Headache Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Paroxysmal Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vomiting, Recurrent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vomiting, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Bronchiolitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchiolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Thrombophlebitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thrombophlebitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Mycobacterium Avium Complex Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterium Avium Complex Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Hypoglycemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Thromboembolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thromboembolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Viral Skin Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Staphylococcal Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Gram-Negative Bacterial Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gram-Negative Bacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Loss Of Toenails And Fingernails Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Loss Of Toenails And Fingernails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Pharyngitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Pharyngitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Deep Vein Thrombosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Low Back Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Shingles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Shingles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chronic recurrent multifocal osteomyelitis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic recurrent multifocal osteomyelitis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hyper IgE recurrent infection syndrome 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyper IgE recurrent infection syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyper IgE recurrent infection syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic recurrent multifocal osteomyelitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic recurrent multifocal osteomyelitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Recurrent hypersomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Recurrent corneal erosion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial recurrent erosion dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial recurrent erosion dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyper IgE recurrent infection syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Recurrent axon collateral Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Recurrent fever Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent subcortical infarcts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent subcortical infarcts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyper-IgE recurrent infection syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyper-IgE recurrent infection syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epithelial recurrent erosion dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epithelial recurrent erosion dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent pancreatitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent infections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute Recurrent Myoglobinuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute Recurrent Myoglobinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent respiratory infections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent respiratory infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent Neisseria infections due to factor D deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent Neisseria infections due to factor D deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Otitis media (recurrent) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Otitis media (chronic/recurrent) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (chronic/recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Broad depression or major depressive disorder (recurrent) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or major depressive disorder (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrent major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrent major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
North american indian childhood cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Alternating hemiplegia of childhood Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercalciuria, childhood, self-limiting Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Childhood hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alternating hemiplegia of childhood 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.
North American Indian Childhood Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophies of Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Diagnosed in Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset.
Alternating hemiplegia of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset.
Arthropathy, progressive pseudorheumatoid, of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.
Hypophosphatasia, Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Childhood from the curated CTD Gene-Disease Associations dataset.
alternating hemiplegia of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
childhood oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood type dermatomyositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood kidney neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood disintegrative disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood malignant schwannoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood kidney cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood endodermal sinus tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alternating hemiplegia of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood pilocytic astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
severe childhood thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood b-cell non-hodgkin's lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphoblastic leukemia (childhood) Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphoblastic leukemia (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood only) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temperament in early childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease temperament in early childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood absence epilepsy. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood b-cell precursor acute lymphoblastic leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood b-cell precursor acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophies of childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood brain tumors ; residential insecticide exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood & adult) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood atopic asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood brain tumor Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, childhood acute lymphoblastic Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute lymphoblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood acute lymphoblastic leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood-onset mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood-onset mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood maltreatment Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood maltreatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (childhood) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, childhood acute; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood idiopathic thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma and ige in childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma and ige in childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy 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.
asthma (childhood onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term childhood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Fractional exhaled nitric oxide (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Acute lymphoblastic leukemia (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Intelligence (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Intelligence (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood, severe) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
childhood-onset short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in childhood Gene Set From HPO Gene-Disease Associations genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood-onset truncal obesity Gene Set From HPO Gene-Disease Associations genes associated with the childhood-onset truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset short-limb short stature Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of ability to walk in early childhood Gene Set From HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inability to walk by childhood/adolescence Gene Set From HPO Gene-Disease Associations genes associated with the inability to walk by childhood/adolescence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
platyspondyly (childhood) Gene Set From HPO Gene-Disease Associations genes associated with the platyspondyly (childhood) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spinal Muscular Atrophies of Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lead Poisoning, Nervous System, Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lead Poisoning, Nervous System, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Schizophrenia, Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Schizophrenia, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hypophosphatasia, childhood Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatasia, childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
hepatocellular carcinoma, childhood type Gene Set From OMIM Gene-Disease Associations genes associated with the hepatocellular carcinoma, childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.
alternating hemiplegia of childhood 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, childhood absence, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
transient erythroblastopenia of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the transient erythroblastopenia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
cirrhosis, north american indian childhood type Gene Set From OMIM Gene-Disease Associations genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.
alternating hemiplegia of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
arthropathy, progressive pseudorheumatoid, of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
polyarteritis nodosa, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the polyarteritis nodosa, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
Childhood Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Liposarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Osteosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Neuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Kidney Wilms Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Myelodysplastic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cytopenia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Megakaryoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Megakaryoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Alveolar Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Alveolar Soft Part Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diffuse Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Non-Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pilocytic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Synovial Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Synovial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood T Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Newly Diagnosed Childhood Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Newly Diagnosed Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Metastatic Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Steroid Resistant Nephrotic Syndrome Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Steroid Resistant Nephrotic Syndrome Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Burkitt Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Undifferentiated Pleomorphic Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Undifferentiated Pleomorphic Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Supratentorial Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Renal Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Monocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myelomonocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myelomonocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Burkitt Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hematopoietic Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hematopoietic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pre-B Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pre-B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Oligodendroglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ataxia With Central Nervous System Hypomyelinization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Craniopharyngioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Eosinophilic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Eosinophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Embryonal Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ganglioneuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioneuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Leiomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leiomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyarteritis Nodosa, Childhood-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyarteritis Nodosa, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Stem Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebral Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Peripheral Nerve Sheath Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gliosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indian Childhood Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Angiosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Testicular Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Teratoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Caries Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Promyelocytic Leukemia With Pml-Rara Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Promyelocytic Leukemia With Pml-Rara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pleomorphic Xanthoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood T Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Epithelioid Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Onset Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Onset Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hypophosphatasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hypophosphatasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Subependymal Giant Cell Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Subependymal Giant Cell Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Oligoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Oligodendroglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade I Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade I Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Langerhans Cell Histiocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Atopic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pineoblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pineoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Monoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Clear Cell Sarcoma Of Soft Parts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Clear Cell Sarcoma Of Soft Parts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Immunoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diffuse Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Oligoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pilomyxoid Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilomyxoid Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Giant Cell Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Giant Cell Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Fibrillary Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Fibrillary Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Desmoplastic Small Round Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Kidney Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Atypical Teratoid/Rhabdoid Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Stem Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gliomatosis Cerebri Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliomatosis Cerebri in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Thyroid Gland Papillary Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Papillary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ovarian Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ovarian Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Epithelioid Hemangioendothelioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Hemangioendothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Hemangiopericytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Hemangiopericytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pleomorphic Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood L2 Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood L2 Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Solid Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Mesenchymal Chondrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mesenchymal Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Erythroid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Erythroid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Liver Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Epilepsy, Benign, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
North American Indian Childhood Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease North American Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercalciuria, Childhood, Self-Limiting Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercalciuria, Childhood, Self-Limiting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Erythroblastopenia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Erythroblastopenia Of Childhood 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.
Childhood Acute Basophilic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Basophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia In Remission Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nodular Sclerosis Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Sclerosis Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Botryoid-Type Embryonal Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Botryoid-Type Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Tic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosis, Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosis, Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophies Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophies Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Bronchiectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Onset Of Psoriasis In Childhood (1-10 Years) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Onset Of Psoriasis In Childhood (1-10 Years) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Conduct Disorder, Childhood-Onset Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Conduct Disorder, Childhood-Onset Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gemistocytic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gemistocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood-Onset Spasticity With Hyperglycinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Spasticity With Hyperglycinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Childhood-Onset, With Psychomotor Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Childhood-Onset, With Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Celiac Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade Ii Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Ii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Focal Epilepsy, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metastatic Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gastrointestinal Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progeria Syndrome, Childhood-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progeria Syndrome, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Fibrous Histiocytoma Of Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Fibrous Histiocytoma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Small Intestinal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Small Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Colorectal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Thyroid Gland Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade Iii Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Iii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Mixed Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Epilepsy, Myoclonic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Supratentorial Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexplained Death In Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Leukemia In Remission Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Infratentorial Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Infratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Disintegrative Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Disintegrative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pneumonia Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pneumonia Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Choroid Plexus Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Choroid Plexus Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood-Onset Short-Trunk Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebellar Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death In Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Solid Neoplasm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood-Onset Truncal Obesity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood-Onset Truncal Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Overweight Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Overweight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Aggression Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Aggression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Selective Mutism Specific To Childhood And Adolescence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Selective Mutism Specific To Childhood And Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Ability To Walk In Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Onset Short-Limb Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Convulsion In Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Convulsion In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Inability To Walk By Childhood/Adolescence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inability To Walk By Childhood/Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Onset Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Alternating hemiplegia of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Childhood type dermatomyositis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Childhood type dermatomyositis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute lymphocytic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood endodermal sinus tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood B-cell acute lymphoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood B-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood fibrosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood low-grade glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood low-grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood disintegrative disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute myeloid leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood type dermatomyositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood malignant schwannoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Systemic Epstein-Barr virus positive T-cell lymphoma of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Systemic Epstein-Barr virus positive T-cell lymphoma of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood T-cell acute lymphoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood T-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood brain stem neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood brain stem glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood osteosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood germ cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood astrocytic tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood astrocytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood infratentorial ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood leptomeningeal melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leptomeningeal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood angiosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood pilocytic astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alternating hemiplegia of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 28, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood hypophosphatasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset neurodegeneration with brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood central nervous system embryonal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood hepatocellular carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hepatocellular carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute megakaryoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute megakaryoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 35, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood supratentorial ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood supratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood testicular germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malignant childhood germ cell neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant childhood germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood infratentorial neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood optic nerve glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney angiomyolipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ovarian dysgerminoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian dysgerminoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ovarian germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood onset hearing loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood apraxia of speech Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood apraxia of speech phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-childhood-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glaucoma of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glaucoma of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alternating hemiplegia of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset GLUT1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy 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.
Childhood neoplasm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood neoplasm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe underweight in infancy childhood and adolescence Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe underweight in infancy childhood and adolescence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood ganglioglioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood ganglioglioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood myocerebrohepatopathy spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood myocerebrohepatopathy spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive bulbar palsy of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood Onset Dystonias Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset Dystonias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood kidney cell carcinoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood kidney cell carcinoma 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.
Childhood-onset motor and cognitive regression syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile or childhood onset neurodegenerative disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary North American Indian childhood cirrhosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary North American Indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sudden unexplained death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood-onset autosomal recessive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
B-cell childhood acute lymphoblastic leukemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the B-cell childhood acute lymphoblastic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood Onset VCP-related Neurodevelopmental Disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset VCP-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disabling pansclerotic morphea of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Disabling pansclerotic morphea of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign childhood epilepsy with centro-temporal spikes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cutaneous mastocytosis (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous mastocytosis (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
First fracture in long-term childhood cancer survivors (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First fracture in long-term childhood cancer survivors (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood body mass index Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anthracycline-induced cardiotoxicity in childhood cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anthracycline-induced cardiotoxicity in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obesity in adult survivors of childhood cancer exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obesity in adult survivors of childhood cancer not exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer not exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early childhood aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early childhood aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Middle childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood ear infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ear infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood maltreatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood maltreatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Meningococcal C functional antibody titers post childhood immunization Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma onset (childhood vs adult) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma onset (childhood vs adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood onset ulcerative colitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset ulcerative colitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fractional exhaled nitric oxide (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fasting plasma glucose (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting plasma glucose (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) x early life tobacco smoke interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) x early life tobacco smoke interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood onset type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia in childhood (B cell precursor) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia in childhood (B cell precursor) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Premature menopause in childhood cancer survivors Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Premature menopause in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood steroid-sensitive nephrotic syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood steroid-sensitive nephrotic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to placebo treatment in childhood asthma (FVC change) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to placebo treatment in childhood asthma (FVC change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Self-reported childhood asthma in adult smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported childhood asthma in adult smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia (adult vs childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (adult vs childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe exacerbations in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood dental caries in primary teeth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in primary teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood dental caries in permanent teeth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in permanent teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cisplatin-induced hearing loss in childhood cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Recurrent Childhood Medulloblastoma Gene Set

Recurrent Medulloblastoma Gene Set

childhood medulloblastoma Gene Set

Childhood Medulloblastoma Gene Set

Childhood medulloblastoma Gene Set

recurrent infections in infancy and early childhood Gene Set

Recurrent Childhood Acute Lymphoblastic Leukemia Gene Set

Recurrent Childhood Glioblastoma Gene Set

Recurrent Childhood Hepatocellular Carcinoma Gene Set

Recurrent Childhood Rhabdomyosarcoma Gene Set

Recurrent Childhood Anaplastic Astrocytoma Gene Set

Recurrent Infections In Infancy And Early Childhood Gene Set

MYC-20876797-MEDULLOBLASTOMA-HUMAN Gene Set

Medulloblastoma Gene Set

melanotic medulloblastoma Gene Set

nodular medulloblastoma Gene Set

large cell medulloblastoma Gene Set

cerebellar medulloblastoma Gene Set

adult medulloblastoma Gene Set

medulloblastoma Gene Set

brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set

cerebellar neoplasms; medulloblastoma Gene Set

medulloblastoma; nijmegen breakage syndrome Gene Set

medulloblastoma Gene Set

Mel-18_KD_GDS2724_103_human_DAOY medulloblastoma cells Gene Set

Bmi-1_KD_GDS2724_102_human_DAOY medulloblastoma cells Gene Set

ALK_KD_GDS2724_105_human_DAOY medulloblastoma cells Gene Set

OTX2_silencing_GDS4472_136_human_D425 medulloblastoma (MB) cells Gene Set

medulloblastoma Gene Set

Medulloblastoma Gene Set

increased medulloblastoma incidence Gene Set

medulloblastoma Gene Set

medulloblastoma, desmoplastic Gene Set

{medulloblastoma} Gene Set

medulloblastoma cell Gene Set

medulloblastoma cell Gene Set

medulloblastoma cell line Gene Set

Adult Medulloblastoma Gene Set

Medulloblastoma Gene Set

Cerebellar Medulloblastoma Gene Set

Desmoplastic Medulloblastoma Gene Set

Melanotic Medulloblastoma Gene Set

Classic Medulloblastoma Gene Set

Large Cell/Anaplastic Medulloblastoma Gene Set

Large Cell Medulloblastoma Gene Set

Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma Gene Set

MYC-20876797-MEDULLOBLASTOMA-HUMAN Gene Set

increased medulloblastoma incidence Gene Set

Cerebellar medulloblastoma Gene Set

Medulloblastoma Gene Set

desmoplastic/nodular medulloblastoma Gene Set

Adult medulloblastoma Gene Set

Melanotic medulloblastoma Gene Set

Cerebellar vermis medulloblastoma Gene Set

Large cell medulloblastoma Gene Set

Medulloblastoma SHH activated Gene Set

Medulloblastoma SHH activated and TP53 wild-type Gene Set

Medulloblastoma WNT activated Gene Set

Medulloblastoma non-WNT/non-SHH Gene Set

Medulloblastoma SHH activated and TP53 mutant Gene Set

Brain stem medulloblastoma Gene Set

Medulloblastoma cell Gene Set

Medulloblastoma cell line Gene Set

Medulloblastoma cell Gene Set

Medulloblastoma Gene Set

Desmoplastic/nodular medulloblastoma Gene Set

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

Myoglobinuria, acute recurrent, autosomal recessive Gene Set

Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set

Benign recurrent intrahepatic cholestasis 2 Gene Set

Hypotrichosis and recurrent skin vesicles Gene Set

Hydatidiform mole, recurrent, 2 Gene Set

recurrent axon collateral Gene Set

Hypotrichosis And Recurrent Skin Vesicles Gene Set

Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set

CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene Set

Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene Set

Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set

Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set