down syndrome; fetal diseases

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Results for "down syndrome; fetal diseases": 1001 gene sets

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down syndrome; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; ehlers-danlos syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma Gene Set From GAD Gene-Disease Associations genes associated with the disease bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; alcoholism; liver diseases; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; infant, premature, diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Transient Myeloproliferative Disorder of Down Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Transient Myeloproliferative Disorder of Down Syndrome from the curated CTD Gene-Disease Associations dataset.
Leukemia, Megakaryoblastic, of Down Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukemia, Megakaryoblastic, of Down Syndrome from the curated CTD Gene-Disease Associations dataset.
Down Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Down Syndrome from the curated CTD Gene-Disease Associations dataset.
down syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease down syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
down syndrome; hirschsprung disease; nondisjunction, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; hirschsprung disease; nondisjunction, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; down syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; nondisjunction, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; nondisjunction, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; leukemia, myeloid; myeloid leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; hepatitis b; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; hepatitis b; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; leukemia, myeloid, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; down syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; down syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease down's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; down syndrome; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; down syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; down syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Down Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Down Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
down syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the down syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leukemia, transient, of down syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, transient, of down syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Down syndrome Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Down syndrome from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Down Syndrome Critical Region Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Down Syndrome Critical Region in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myeloid Leukemia Associated With Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myeloid Leukemia Associated With Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Myeloproliferative Disorder Of Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Myeloproliferative Disorder Of Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myeloid Proliferations Associated With Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myeloid Proliferations Associated With Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Down syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Down syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Down syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Down syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myeloid leukemia associated with Down Syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid leukemia associated with Down Syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Down syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Down syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute megakaryoblastic leukemia in down syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute megakaryoblastic leukemia in down syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic; rheumatic diseases; rheumatism; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic; rheumatic diseases; rheumatism; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; liver diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; liver diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Fetal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Diseases from the curated CTD Gene-Disease Associations dataset.
fetal diseases; hemoglobinopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hemoglobinopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; fetal diseases; malnutrition; starvation Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; fetal diseases; malnutrition; starvation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; hemophilia a Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hemophilia a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta thalassemia; beta-thalassemia; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; periodontal diseases; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Fetal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway Gene Set From Biocarta Pathways proteins participating in the phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway pathway from the Biocarta Pathways dataset.
down Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term down in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Down Syndrome_CNS - Brain - Cerebellum (MMHCC)_GSE1611 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Down Syndrome_CNS - Brain - Cerebellum (MMHCC)_GSE1611 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Down Syndrome_Brain_GSE5390 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Down Syndrome_Brain_GSE5390 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Down Syndrome_Fetus_GSE10758 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Down Syndrome_Fetus_GSE10758 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
NET1_KD_GDS4196_436_human_AGS - gastric adenocarcinoma cells - (63 shRNA Knock-Down) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NET1_KD_GDS4196_436_human_AGS - gastric adenocarcinoma cells - (63 shRNA Knock-Down) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
NET1_KD_GDS4196_437_human_AGS - gastric adenocarcinoma cells - (65 shRNA Knock-Down) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NET1_KD_GDS4196_437_human_AGS - gastric adenocarcinoma cells - (65 shRNA Knock-Down) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
energy coupled proton transport, down electrochemical gradient Gene Set From GO Biological Process Annotations 2015 genes participating in the energy coupled proton transport, down electrochemical gradient biological process from the curated GO Biological Process Annotations 2015 dataset.
down-sloping shoulders Gene Set From HPO Gene-Disease Associations genes associated with the down-sloping shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Down-regulated-in-metastasis protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Down-regulated-in-metastasis protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal hair-down neuron morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hair-down neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent hair-down neurons Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Nef Mediated CD8 Down-regulation Gene Set From Reactome Pathways 2014 proteins participating in the Nef Mediated CD8 Down-regulation pathway from the Reactome Pathways dataset.
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters Gene Set From Reactome Pathways 2014 proteins participating in the Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters pathway from the Reactome Pathways dataset.
Nef Mediated CD4 Down-regulation Gene Set From Reactome Pathways 2014 proteins participating in the Nef Mediated CD4 Down-regulation pathway from the Reactome Pathways dataset.
Down-Sloping Shoulders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Down-Sloping Shoulders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
absent hair-down neurons Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
down-turned corners of mouth Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the down-turned corners of mouth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set From Reactome Pathways 2024 proteins participating in the FBXL7 down-regulates AURKA during mitotic entry and in early mitosis pathway from the Reactome Pathways 2024 dataset.
Nef Mediated CD4 Down-regulation Gene Set From Reactome Pathways 2024 proteins participating in the Nef Mediated CD4 Down-regulation pathway from the Reactome Pathways 2024 dataset.
Nef Mediated CD8 Down-regulation Gene Set From Reactome Pathways 2024 proteins participating in the Nef Mediated CD8 Down-regulation pathway from the Reactome Pathways 2024 dataset.
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters Gene Set From Reactome Pathways 2024 proteins participating in the Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters pathway from the Reactome Pathways 2024 dataset.
PTK6 Down-Regulation Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Down-Regulation pathway from the Reactome Pathways 2024 dataset.
TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PMC9633745-mmc3.xlsx-Table_S2-Down-regulated_in_MSC-2_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC9633745-mmc3.xlsx-Table_S2-Down-regulated_in_MSC-2_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC9974104-jci-133-159940-s017.xlsx-GT3-INCP-GATA3_Co-down-Gene_ID_GATA3 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC9974104-jci-133-159940-s017.xlsx-GT3-INCP-GATA3_Co-down-Gene_ID_GATA3 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC9974104-jci-133-159940-s017.xlsx-GT3-INCP-GATA3_Co-down-Symbol_GATA3 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC9974104-jci-133-159940-s017.xlsx-GT3-INCP-GATA3_Co-down-Symbol_GATA3 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC9530161-41419_2022_5296_MOESM2_ESM.xlsx-Tab9_KDM5C-KD-down-DKD-rescued-Table_9_Down-regluted_genes_in_KDM5C-KD_and_rescued_genes_in_DKD_AR Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC9530161-41419_2022_5296_MOESM2_ESM.xlsx-Tab9_KDM5C-KD-down-DKD-rescued-Table_9_Down-regluted_genes_in_KDM5C-KD_and_rescued_genes_in_DKD_AR transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC8755441-mmc3.xlsx-IRF1-Down-Symbol_IRF1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC8755441-mmc3.xlsx-IRF1-Down-Symbol_IRF1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC8755441-mmc3.xlsx-IRF7-down-Symbol_IRF7 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC8755441-mmc3.xlsx-IRF7-down-Symbol_IRF7 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC8040704-jcav12p2673s2.xlsx-Down-regulated_genes_in_EBF1-Unnamed_0_EBF1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC8040704-jcav12p2673s2.xlsx-Down-regulated_genes_in_EBF1-Unnamed_0_EBF1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC8040704-jcav12p2673s2.xlsx-Down-regulated_genes_in_EBF1-Unnamed_5_EBF1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC8040704-jcav12p2673s2.xlsx-Down-regulated_genes_in_EBF1-Unnamed_5_EBF1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6344081-elife-40364-supp8.xlsx-PLZF-Si-diff-expressed-gen-Down-Symbol_ZBTB16 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6344081-elife-40364-supp8.xlsx-PLZF-Si-diff-expressed-gen-Down-Symbol_ZBTB16 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC4653014-oncotarget-06-20404-s004.xls-Down-regulated_in_AFAP1-AS1_KD-Unnamed_1_AR Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC4653014-oncotarget-06-20404-s004.xls-Down-regulated_in_AFAP1-AS1_KD-Unnamed_1_AR transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC3029394-pone.0016617.s001.xls-Down-regulated-Table_S1_Genes_down-regulated_by_SOX2_over-expression_0_5-fold_SOX2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC3029394-pone.0016617.s001.xls-Down-regulated-Table_S1_Genes_down-regulated_by_SOX2_over-expression_0_5-fold_SOX2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC5798892-41421_2017_3_MOESM8_ESM.xlsx-down-regulated-Supplementary_Table_S3_Up-_and_downregulated_genes_in_ATF6-_-_hMSCs_compared_to_ATF6_hMSCs_late_passage_ATF6 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC5798892-41421_2017_3_MOESM8_ESM.xlsx-down-regulated-Supplementary_Table_S3_Up-_and_downregulated_genes_in_ATF6-_-_hMSCs_compared_to_ATF6_hMSCs_late_passage_ATF6 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC5259899-13287_2016_455_MOESM2_ESM.xlsx-Down-regulated-Supplementary_Table_S2_Down-reguated_genes_expression_in_MESP1_negative_cells_MESP1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC5259899-13287_2016_455_MOESM2_ESM.xlsx-Down-regulated-Supplementary_Table_S2_Down-reguated_genes_expression_in_MESP1_negative_cells_MESP1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC4909989-ncomms11840-s2.xlsx-down-regulate-TEAD4-FL_YAP_TEAD4 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC4909989-ncomms11840-s2.xlsx-down-regulate-TEAD4-FL_YAP_TEAD4 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC4909989-ncomms11840-s2.xlsx-down-regulate-TEAD4-S_YAP_TEAD4 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC4909989-ncomms11840-s2.xlsx-down-regulate-TEAD4-S_YAP_TEAD4 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC11799530-12276_2024_1380_MOESM1_ESM.xlsx-COMMON_KD-UP_and_OE-DOWN-86_common_elements_in_kd-up_and_oe-down_AR Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11799530-12276_2024_1380_MOESM1_ESM.xlsx-COMMON_KD-UP_and_OE-DOWN-86_common_elements_in_kd-up_and_oe-down_AR transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-F_48h_2-down-regulated_PDX1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-F_48h_2-down-regulated_PDX1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-F_72h_2-down-regulated_PDX1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-F_72h_2-down-regulated_PDX1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-S_48h_2-down-regulated_PDX1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-S_48h_2-down-regulated_PDX1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-S_72h_2-down-regulated_PDX1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12621392-12864_2025_12212_MOESM2_ESM.xlsx-GSF-S_72h_2-down-regulated_PDX1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; sarcoidosis; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; sarcoidosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; hypersensitivity; respiratory tract diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
duodenal diseases; helicobacter infections; stomach diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease duodenal diseases; helicobacter infections; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; carcinoma, hepatocellular; lcc - liver cell carcinoma; liver diseases, alcoholic; liver neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; carcinoma, hepatocellular; lcc - liver cell carcinoma; liver diseases, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenoleukodystrophy; demyelinating diseases; metabolic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenoleukodystrophy; demyelinating diseases; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cardiovascular diseases; ischemia; stroke; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cardiovascular diseases; ischemia; stroke; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anus diseases; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease anus diseases; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occupational diseases; respiratory tract diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease occupational diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; hemochromatosis; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; hemochromatosis; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erythema; rare diseases; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease erythema; rare diseases; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus, type 2; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus, type 2; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colonic diseases; crohn disease; ileal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease colonic diseases; crohn disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; joint diseases; rheumatic diseases; rheumatism Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; joint diseases; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; rheumatic diseases; rheumatism Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; thyroid diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus; kidney diseases; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus; kidney diseases; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; skin diseases, vesiculobullous Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; skin diseases, vesiculobullous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; hypertension; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; intermittent claudication; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; peripheral vascular diseases; vitreous hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; peripheral vascular diseases; vitreous hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic Gene Set From GAD Gene-Disease Associations genes associated with the disease heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; skin diseases, genetic; vitiligo Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; skin diseases, genetic; vitiligo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; metabolic diseases; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; metabolic diseases; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; alcoholism; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; cardiovascular diseases; diabetes mellitus, type 2; hypertension; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus, type 2; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asymptomatic diseases; cyst; cysts; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease asymptomatic diseases; cyst; cysts; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; carotid artery diseases; hyperlipoproteinemia type i; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; carotid artery diseases; hyperlipoproteinemia type i; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; chagas disease; communicable diseases; dengue; leishmaniasis, cutaneous; myasthenia gravis; pemphigus; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chagas disease; communicable diseases; dengue; leishmaniasis, cutaneous; myasthenia gravis; pemphigus; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; neurodegenerative diseases; prion diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; neurodegenerative diseases; prion diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; lung diseases; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; lung diseases; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Pierre Robin syndrome with fetal chondrodysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pierre Robin syndrome with fetal chondrodysplasia from the curated CTD Gene-Disease Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Persistent Fetal Circulation Syndrome from the curated CTD Gene-Disease Associations dataset.
persistent fetal circulation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease persistent fetal circulation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal anticonvulsant syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal anticonvulsant syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Persistent Fetal Circulation Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Alcohol Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Alcohol Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
?fetal hydantoin syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?fetal hydantoin syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Fetal Circulation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Alcohol Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Fetal Alcohol Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Hydantoin Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Hydantoin Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent fetal circulation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent fetal circulation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal valproate syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal valproate syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal akinesia deformation sequence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal akinesia deformation sequence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal encasement syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal encasement syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal akinesia deformation sequence syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal akinesia deformation sequence syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal akinesia-cerebral and retinal hemorrhage syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia-cerebral and retinal hemorrhage syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; nervous system diseases; ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; nervous system diseases; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone marrow diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; disease susceptibility; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; disease susceptibility; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone marrow diseases; dyskeratosis congenita; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; dyskeratosis congenita; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; behcet syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; behcet syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cockayne syndrome; genetic diseases, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease cockayne syndrome; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pancreatic diseases; pancreatitis; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease pancreatic diseases; pancreatitis; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; lung diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; lung diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
constipation; dyspepsia; gastrointestinal diseases; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease constipation; dyspepsia; gastrointestinal diseases; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; dyslipidemias; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; dyslipidemias; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cushing syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cushing syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
communicable diseases; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease communicable diseases; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; cardiovascular diseases; coronary artery disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; cardiovascular diseases; coronary artery disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; pelvic pain; prostatitis; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; pelvic pain; prostatitis; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; cardiovascular diseases; lupus erythematosus, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; cardiovascular diseases; lupus erythematosus, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic diseases; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic diseases; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic diseases, x-linked; rett syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic diseases, x-linked; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; periodontal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; periodontal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nervous system diseases; rett syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nervous system diseases; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
connective tissue diseases; ectopia lentis; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; ectopia lentis; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cardiovascular diseases; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cardiovascular diseases; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic diseases, inborn; syndrome; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; syndrome; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; lymphomatoid granulomatosis; sarcoidosis; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; lymphomatoid granulomatosis; sarcoidosis; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; corneal diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; corneal diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; cardiovascular diseases; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; cardiovascular diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms ; osteoporosis; alzheimer diseasey; cardiovascular diseases; metabolic syndrome x; diabetes complications Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms ; osteoporosis; alzheimer diseasey; cardiovascular diseases; metabolic syndrome x; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; metabolic syndrome x; obesity, morbid Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; metabolic syndrome x; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; eye diseases; Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; eye diseases; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; stevens-johnson syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fetal hemoglobin quantitative trait locus 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fetal hemoglobin quantitative trait locus 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fetal hemoglobin quantitative trait locus 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fetal hemoglobin quantitative trait locus 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fetal Resorption Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Resorption from the curated CTD Gene-Disease Associations dataset.
Fetal Alcohol Spectrum Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Growth Retardation from the curated CTD Gene-Disease Associations dataset.
Fetal Weight Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Weight from the curated CTD Gene-Disease Associations dataset.
Fetal Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Death from the curated CTD Gene-Disease Associations dataset.
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor from the curated CTD Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Nutrition Disorders from the curated CTD Gene-Disease Associations dataset.
Fetal Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Distress from the curated CTD Gene-Disease Associations dataset.
Fetal Hemoglobin Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Fetal Hemoglobin in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal erythroblastosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal erythroblastosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal membranes, premature rupture; Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal nutrition disorders; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal nutrition disorders; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal membranes, premature rupture; premature birth; uterine prolapse Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; premature birth; uterine prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications 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.
fetal hemoglobin levels Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal hemoglobin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
embryo loss; fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, late Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal hemoglobin Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal hemoglobin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal akinesia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal akinesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, early Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal membranes, premature rupture; obstetric labor, premature Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; obstetric labor, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism 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.
fetal membrane rupture Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membrane rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss ; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss ; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pre-eclampsia 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.
erythroblastosis, fetal Gene Set From GAD Gene-Disease Associations genes associated with the disease erythroblastosis, fetal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal membranes, premature rupture Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal membranes, premature rupture; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial vaginosis; fetal membranes, premature rupture; vaginosis, bacterial Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term fetal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Zfp36l2_deficiency_GDS3574_153_mouse_E14.5 fetal liver Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Zfp36l2_deficiency_GDS3574_153_mouse_E14.5 fetal liver gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
E2A_KO_GSE43224_679_mouse_DN2 cells from WT and E2A-deficient murine fetal thymi Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the E2A_KO_GSE43224_679_mouse_DN2 cells from WT and E2A-deficient murine fetal thymi gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
fetal process involved in parturition Gene Set From GO Biological Process Annotations 2015 genes participating in the fetal process involved in parturition biological process from the curated GO Biological Process Annotations 2015 dataset.
Fetal hemoglobin levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fetal hemoglobin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
fetal polyuria Gene Set From HPO Gene-Disease Associations genes associated with the fetal polyuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
premature birth following premature rupture of fetal membranes Gene Set From HPO Gene-Disease Associations genes associated with the premature birth following premature rupture of fetal membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the fetal cardiovascular system Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the fetal cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal ultrasound soft marker Gene Set From HPO Gene-Disease Associations genes associated with the fetal ultrasound soft marker phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fetal movement Gene Set From HPO Gene-Disease Associations genes associated with the decreased fetal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal akinesia sequence Gene Set From HPO Gene-Disease Associations genes associated with the fetal akinesia sequence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal ascites Gene Set From HPO Gene-Disease Associations genes associated with the fetal ascites phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal cystic hygroma Gene Set From HPO Gene-Disease Associations genes associated with the fetal cystic hygroma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal megacystis Gene Set From HPO Gene-Disease Associations genes associated with the fetal megacystis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Fetal Macrosomia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Macrosomia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Weight Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Weight phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Erythroblastosis, Fetal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Erythroblastosis, Fetal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Growth Retardation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Growth Retardation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Membranes, Premature Rupture Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Membranes, Premature Rupture phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Nutrition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal septation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal embryonic/fetal subventricular zone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic/fetal subventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal bleb Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fetal bleb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal placenta fetal blood space morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal ductus arteriosus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent fetal ductus arteriosus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent fetal ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal liver hematopoietic progenitor cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal liver hematopoietic progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal derived definitive erythrocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal akinesia deformation sequence Gene Set From OMIM Gene-Disease Associations genes associated with the fetal akinesia deformation sequence phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 2 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 4 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
[hereditary persistence of fetal hemoglobin] Gene Set From OMIM Gene-Disease Associations genes associated with the [hereditary persistence of fetal hemoglobin] phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 1 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary persistence of fetal hemoglobin Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary persistence of fetal hemoglobin phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fetal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Fetal Heart Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Heart relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Fetal Brain Male Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Brain Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Fetal Lung Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Lung relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Fetal Kidney Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Kidney relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
fetal cell line Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fetal cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
fetal membrane Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fetal membrane from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
fetal serum Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal serum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
fetal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
fetal membrane Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal membrane in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Fetal growth restriction Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Fetal growth restriction from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Fetal Resorption Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Resorption in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Distress Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Megacystis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Megacystis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Abnormality Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Ascites Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Ascites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Persistence Of Fetal Hemoglobin Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Persistence Of Fetal Hemoglobin Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Anencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Anencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Hypoxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Hypoxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrapartum Fetal Hypoxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrapartum Fetal Hypoxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Pyelectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Pyelectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Cerebral Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Cerebral Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Fetal Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Fetal Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Lung Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Lung Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Rhabdomyoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Rhabdomyoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Preterm Premature Rupture Of Fetal Membranes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Preterm Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Fetal Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Fetal Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Without Mention Of Light-For-Dates Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition Without Mention Of Light-For-Dates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Thrombotic Vasculopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Thrombotic Vasculopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Macrosomia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Macrosomia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Fetal Pyelectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Fetal Pyelectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Nutrition Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Microcephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Heart Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Fetal Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Fetal Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Membranes, Premature Rupture Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Membranes, Premature Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Severe Fetal Akinesia Sequence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Severe Fetal Akinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hemoglobin Determination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hemoglobin Determination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Polyuria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Polyuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hydrops (In Some Patients) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hydrops (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stomach Bubble On Fetal Sonography Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stomach Bubble On Fetal Sonography in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Premature Birth Following Premature Rupture Of Fetal Membranes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Birth Following Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hydrops (In Perinatal Or Congenital Neuromuscular Forms) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hydrops (In Perinatal Or Congenital Neuromuscular Forms) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Mummification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Mummification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hemoglobin Quantitative Trait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hemoglobin Quantitative Trait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Descent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Descent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Fetal Femur Length Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fetal Femur Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
DMRT1-21621532-FETAL-OVARY Gene Set From ChEA Transcription Factor Targets 2022 target genes of the DMRT1-21621532-FETAL-OVARY transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
CTNNB1-20615089-FETAL-BRAIN-HUMAN Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CTNNB1-20615089-FETAL-BRAIN-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
TAL1-20566737-PRIMARY-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the TAL1-20566737-PRIMARY-FETAL-LIVER-ERYTHROID-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
decreased fetal weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fetal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fetal bleb Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fetal bleb phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal embryonic/fetal subventricular zone morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryonic/fetal subventricular zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal placenta fetal blood space morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal growth/weight/body size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal Leydig cell differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal Leydig cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent fetal ductus arteriosus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fetal ductus arteriosus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal cardiomyocyte apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal ductus arteriosus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal liver hematopoietic progenitor cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal liver hematopoietic progenitor cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte physiology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal derived definitive erythrocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal derived definitive erythrocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Fetal Development - L1 - Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ganglion cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Adrenocortical cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Adrenocortical cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - STC2_TLX1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - STC2_TLX1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Satellite cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Satellite cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Sympathoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Sympathoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ureteric bud cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ureteric bud cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Limbic system neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Limbic system neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Inhibitory interneurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Inhibitory interneurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Endocardial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Endocardial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Photoreceptor cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SLC24A4_PEX5L positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SLC24A4_PEX5L positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Excitatory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Excitatory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SKOR2_NPSR1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SKOR2_NPSR1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Hepatoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Hepatoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Thymocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Thymocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Purkinje neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Purkinje neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Syncytiotrophoblasts and villous cytotrophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Syncytiotrophoblasts and villous cytotrophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Mesangial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Mesangial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Intestinal epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Granule neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Granule neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Horizontal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Inhibitory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Inhibitory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Islet endocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Islet endocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Amacrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Unipolar brush cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Unipolar brush cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - MUC13_DMBT1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - MUC13_DMBT1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Acinar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Acinar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Metanephric cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Metanephric cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ductal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ductal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Cardiomyocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Cardiomyocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Goblet cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Goblet cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Extravillous trophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Extravillous trophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Epicardial fat cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Parietal and chief cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Parietal and chief cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Stellate cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Stellate cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - IGFBP1_DKK1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - IGFBP1_DKK1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Bipolar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Bipolar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PAEP_MECOM positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PAEP_MECOM positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Hematopoietic stem cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Hematopoietic stem cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lens fibre cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CCL19_CCL21 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CCL19_CCL21 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Trophoblast giant cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Trophoblast giant cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SLC26A4_PAEP positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SLC26A4_PAEP positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Thymic epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Thymic epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PDE11A_FAM19A2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Antigen presenting cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Antigen presenting cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SATB2_LRRC7 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SATB2_LRRC7 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ELF3_AGBL2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ELF3_AGBL2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CLC_IL5RA positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CLC_IL5RA positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PDE1C_ACSM3 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PDE1C_ACSM3 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Ganglion cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Adrenocortical cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Adrenocortical cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-STC2_TLX1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-STC2_TLX1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Satellite cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Satellite cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Sympathoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Sympathoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Ureteric bud cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Ureteric bud cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Limbic system neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Limbic system neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Inhibitory interneurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Inhibitory interneurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Endocardial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Endocardial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Photoreceptor cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-SLC24A4_PEX5L positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-SLC24A4_PEX5L positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Excitatory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Excitatory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-SKOR2_NPSR1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-SKOR2_NPSR1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Hepatoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Hepatoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Thymocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Thymocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Purkinje neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Purkinje neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Syncytiotrophoblasts and villous cytotrophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Syncytiotrophoblasts and villous cytotrophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Mesangial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Mesangial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Granule neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Granule neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Horizontal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Inhibitory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Inhibitory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Islet endocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Islet endocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Amacrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Unipolar brush cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Unipolar brush cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-MUC13_DMBT1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-MUC13_DMBT1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Acinar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Acinar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Metanephric cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Metanephric cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Ductal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Ductal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Cardiomyocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Cardiomyocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Goblet cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Goblet cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Extravillous trophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Extravillous trophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Epicardial fat cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Parietal and chief cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Parietal and chief cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Stellate cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Stellate cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-IGFBP1_DKK1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-IGFBP1_DKK1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Bipolar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Bipolar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-PAEP_MECOM positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-PAEP_MECOM positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Hematopoietic stem cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Hematopoietic stem cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Lens fibre cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Trophoblast giant cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Trophoblast giant cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-SLC26A4_PAEP positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-SLC26A4_PAEP positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Thymic epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Thymic epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Antigen presenting cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Antigen presenting cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-SATB2_LRRC7 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-SATB2_LRRC7 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-ELF3_AGBL2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-ELF3_AGBL2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-CLC_IL5RA positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-CLC_IL5RA positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-PDE1C_ACSM3 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-PDE1C_ACSM3 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Circulating fetal cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Circulating fetal cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Circulating fetal cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Circulating fetal cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinoid acid signaling-responsive fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinoid acid signaling-responsive fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Oogenesis phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oogenesis phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Meiotic prophase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Meiotic prophase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mitotic arrest phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Mitotic arrest phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mitotic fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Mitotic fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Migration phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Migration phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Gonadal mitotic phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Gonadal mitotic phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal hepatocyte_Liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal hepatocyte_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal hepatocyte_Liver_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal hepatocyte_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal myoblast_Muscle_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal myoblast_Muscle_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Alternative pathway of fetal androgen synthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Alternative pathway of fetal androgen synthesis pathway from the WikiPathways Pathways 2024 dataset.
Fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal membrane Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Fetal membrane from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Fetal membrane Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fetal membrane in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Fetal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fetal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Fetal serum Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fetal serum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Fetal akinesia deformation sequence Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia deformation sequence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary persistence of fetal hemoglobin Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary persistence of fetal hemoglobin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short fetal femur length Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short fetal femur length phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal cystic hygroma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal cystic hygroma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal akinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal growth restriction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal growth restriction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal and neonatal alloimmune thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal and neonatal alloimmune thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYOM1-related non-immune fetal hydrops Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYOM1-related non-immune fetal hydrops phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal ascites Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal ascites phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Midgestational circulating levels of PCBs (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational circulating levels of PCBs (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Midgestational circulating levels of PBDEs (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational circulating levels of PBDEs (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
High fetal hemoglobin in sickle cell disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High fetal hemoglobin in sickle cell disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Midgestational total 25-hydroxyvitamin D levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Midgestational cytokine/chemokine levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fetal hemoglobin levels in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fetal hemoglobin levels in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fetal hemoglobin levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fetal hemoglobin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lynch syndrome:Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome:Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
IFAP syndrome with or without BRESHECK syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cornelia de lange syndrome; de lange syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; uveomeningoencephalitic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melas syndrome; merrf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angelman syndrome; rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic syndrome ; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart-hand syndrome, holt-oram syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set From OMIM Gene-Disease Associations genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ifap syndrome with or without bresheck syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Crouzon syndrome-acanthosis nigricans syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crouzon syndrome-acanthosis nigricans syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Crouzon syndrome-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mitochondrial diseases Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial diseases phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Liver Diseases, Parasitic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Liver Diseases, Parasitic from the curated CTD Gene-Disease Associations dataset.
Stomach Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stomach Diseases from the curated CTD Gene-Disease Associations dataset.
Carotid Artery Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carotid Artery Diseases from the curated CTD Gene-Disease Associations dataset.
Neuromuscular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuromuscular Diseases from the curated CTD Gene-Disease Associations dataset.
Bile Duct Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile Duct Diseases from the curated CTD Gene-Disease Associations dataset.
Virus Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Virus Diseases from the curated CTD Gene-Disease Associations dataset.
Maxillary Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maxillary Diseases from the curated CTD Gene-Disease Associations dataset.
Rheumatic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Rheumatic Diseases from the curated CTD Gene-Disease Associations dataset.
Thoracic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thoracic Diseases from the curated CTD Gene-Disease Associations dataset.
Foodborne Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foodborne Diseases from the curated CTD Gene-Disease Associations dataset.
Eye Diseases, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases, Hereditary from the curated CTD Gene-Disease Associations dataset.
Prion Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prion Diseases from the curated CTD Gene-Disease Associations dataset.
Skin Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Diseases from the curated CTD Gene-Disease Associations dataset.
Lacrimal Apparatus Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lacrimal Apparatus Diseases from the curated CTD Gene-Disease Associations dataset.
Placenta Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Placenta Diseases from the curated CTD Gene-Disease Associations dataset.
Laryngeal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Laryngeal Diseases from the curated CTD Gene-Disease Associations dataset.
Lung Diseases, Interstitial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lung Diseases, Interstitial from the curated CTD Gene-Disease Associations dataset.
Vestibular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vestibular Diseases from the curated CTD Gene-Disease Associations dataset.
Kidney Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Kidney Diseases from the curated CTD Gene-Disease Associations dataset.
Hair Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hair Diseases from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Infant, Newborn, Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infant, Newborn, Diseases from the curated CTD Gene-Disease Associations dataset.
Periodontal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodontal Diseases from the curated CTD Gene-Disease Associations dataset.
Skin Diseases, Vascular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Diseases, Vascular from the curated CTD Gene-Disease Associations dataset.
Uterine Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Uterine Diseases from the curated CTD Gene-Disease Associations dataset.
Neurodegenerative Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegenerative Diseases from the curated CTD Gene-Disease Associations dataset.
Male Urogenital Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Male Urogenital Diseases from the curated CTD Gene-Disease Associations dataset.
Infant, Premature, Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infant, Premature, Diseases from the curated CTD Gene-Disease Associations dataset.
Bone Marrow Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Marrow Diseases from the curated CTD Gene-Disease Associations dataset.
Dog Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dog Diseases from the curated CTD Gene-Disease Associations dataset.
Hematologic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematologic Diseases from the curated CTD Gene-Disease Associations dataset.
Pleural Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pleural Diseases from the curated CTD Gene-Disease Associations dataset.
Bone Diseases, Metabolic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Metabolic from the curated CTD Gene-Disease Associations dataset.
Occupational Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Occupational Diseases from the curated CTD Gene-Disease Associations dataset.
Eyelid Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eyelid Diseases from the curated CTD Gene-Disease Associations dataset.
Lung Diseases, Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lung Diseases, Obstructive from the curated CTD Gene-Disease Associations dataset.
Mitochondrial Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Diseases from the curated CTD Gene-Disease Associations dataset.
Bone Diseases, Developmental Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Developmental from the curated CTD Gene-Disease Associations dataset.
Gallbladder Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gallbladder Diseases from the curated CTD Gene-Disease Associations dataset.
Eye Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases from the curated CTD Gene-Disease Associations dataset.
Retinal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Diseases from the curated CTD Gene-Disease Associations dataset.
Mouth Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mouth Diseases from the curated CTD Gene-Disease Associations dataset.
Nail Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nail Diseases from the curated CTD Gene-Disease Associations dataset.
Heart Valve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heart Valve Diseases from the curated CTD Gene-Disease Associations dataset.
Ovarian Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ovarian Diseases from the curated CTD Gene-Disease Associations dataset.
Cartilage Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cartilage Diseases from the curated CTD Gene-Disease Associations dataset.
Ileal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ileal Diseases from the curated CTD Gene-Disease Associations dataset.
Vaginal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vaginal Diseases from the curated CTD Gene-Disease Associations dataset.
Lymphatic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lymphatic Diseases from the curated CTD Gene-Disease Associations dataset.
Autoimmune Diseases of the Nervous System Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Autoimmune Diseases of the Nervous System from the curated CTD Gene-Disease Associations dataset.
Basal Ganglia Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Basal Ganglia Diseases from the curated CTD Gene-Disease Associations dataset.
Peripheral Nervous System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.
Testicular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Testicular Diseases from the curated CTD Gene-Disease Associations dataset.
Cranial Nerve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cranial Nerve Diseases from the curated CTD Gene-Disease Associations dataset.
Respiratory Tract Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Respiratory Tract Diseases from the curated CTD Gene-Disease Associations dataset.
Adrenal Cortex Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal Cortex Diseases from the curated CTD Gene-Disease Associations dataset.
Demyelinating Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Demyelinating Diseases from the curated CTD Gene-Disease Associations dataset.
Arterial Occlusive Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arterial Occlusive Diseases from the curated CTD Gene-Disease Associations dataset.
Hereditary Autoinflammatory Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Autoinflammatory Diseases from the curated CTD Gene-Disease Associations dataset.
Cerebellar Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Diseases from the curated CTD Gene-Disease Associations dataset.
Aortic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Diseases from the curated CTD Gene-Disease Associations dataset.
Abducens Nerve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Abducens Nerve Diseases from the curated CTD Gene-Disease Associations dataset.
Prostatic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prostatic Diseases from the curated CTD Gene-Disease Associations dataset.
Niemann-Pick Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Diseases from the curated CTD Gene-Disease Associations dataset.
Gastrointestinal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gastrointestinal Diseases from the curated CTD Gene-Disease Associations dataset.
Intestinal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intestinal Diseases from the curated CTD Gene-Disease Associations dataset.
Muscular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Diseases from the curated CTD Gene-Disease Associations dataset.
Bone Diseases, Endocrine Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Endocrine from the curated CTD Gene-Disease Associations dataset.
Spinal Cord Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Cord Diseases from the curated CTD Gene-Disease Associations dataset.
Stomatognathic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stomatognathic Diseases from the curated CTD Gene-Disease Associations dataset.
Bronchial Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchial Diseases from the curated CTD Gene-Disease Associations dataset.
Peripheral Vascular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Vascular Diseases from the curated CTD Gene-Disease Associations dataset.
Central Nervous System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.
Nervous System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.
Autonomic Nervous System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Autonomic Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.
Optic Nerve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Diseases from the curated CTD Gene-Disease Associations dataset.
Breast Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Breast Diseases from the curated CTD Gene-Disease Associations dataset.
Bone Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases from the curated CTD Gene-Disease Associations dataset.
Brain Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases from the curated CTD Gene-Disease Associations dataset.
Female Urogenital Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Female Urogenital Diseases from the curated CTD Gene-Disease Associations dataset.
Autoimmune Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Autoimmune Diseases from the curated CTD Gene-Disease Associations dataset.
Genetic Diseases, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Diseases, X-Linked from the curated CTD Gene-Disease Associations dataset.
Corneal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Diseases from the curated CTD Gene-Disease Associations dataset.
Cardiovascular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiovascular Diseases from the curated CTD Gene-Disease Associations dataset.
Pituitary Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Diseases from the curated CTD Gene-Disease Associations dataset.
Vascular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vascular Diseases from the curated CTD Gene-Disease Associations dataset.
Urologic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Urologic Diseases from the curated CTD Gene-Disease Associations dataset.
Connective Tissue Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Connective Tissue Diseases from the curated CTD Gene-Disease Associations dataset.
Genetic Diseases, Inborn Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Diseases, Inborn from the curated CTD Gene-Disease Associations dataset.
Lung Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lung Diseases from the curated CTD Gene-Disease Associations dataset.
Liver Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Liver Diseases from the curated CTD Gene-Disease Associations dataset.
Agricultural Workers' Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Agricultural Workers' Diseases from the curated CTD Gene-Disease Associations dataset.
Joint Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Joint Diseases from the curated CTD Gene-Disease Associations dataset.
Genital Diseases, Male Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Male from the curated CTD Gene-Disease Associations dataset.
Tick-Borne Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tick-Borne Diseases from the curated CTD Gene-Disease Associations dataset.
Adrenal Gland Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal Gland Diseases from the curated CTD Gene-Disease Associations dataset.
Penile Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Penile Diseases from the curated CTD Gene-Disease Associations dataset.
Splenic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Splenic Diseases from the curated CTD Gene-Disease Associations dataset.
Myelodysplastic-Myeloproliferative Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myelodysplastic-Myeloproliferative Diseases from the curated CTD Gene-Disease Associations dataset.
Brain Diseases, Metabolic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases, Metabolic from the curated CTD Gene-Disease Associations dataset.
Kidney Diseases, Cystic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Kidney Diseases, Cystic from the curated CTD Gene-Disease Associations dataset.
Deficiency Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deficiency Diseases from the curated CTD Gene-Disease Associations dataset.
Lens Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lens Diseases from the curated CTD Gene-Disease Associations dataset.
Cochlear Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cochlear Diseases from the curated CTD Gene-Disease Associations dataset.
X-Linked Combined Immunodeficiency Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease X-Linked Combined Immunodeficiency Diseases from the curated CTD Gene-Disease Associations dataset.
Immune Complex Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune Complex Diseases from the curated CTD Gene-Disease Associations dataset.
Polycystic Kidney Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic Kidney Diseases from the curated CTD Gene-Disease Associations dataset.
Urinary Bladder Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Urinary Bladder Diseases from the curated CTD Gene-Disease Associations dataset.
Fish Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fish Diseases from the curated CTD Gene-Disease Associations dataset.
Conjunctival Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Conjunctival Diseases from the curated CTD Gene-Disease Associations dataset.
Esophageal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Diseases from the curated CTD Gene-Disease Associations dataset.
Endocrine System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Endocrine System Diseases from the curated CTD Gene-Disease Associations dataset.
Immune System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune System Diseases from the curated CTD Gene-Disease Associations dataset.
Thyroid Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Diseases from the curated CTD Gene-Disease Associations dataset.
Liver Diseases, Alcoholic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Liver Diseases, Alcoholic from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Diseases from the curated CTD Gene-Disease Associations dataset.
Metabolic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metabolic Diseases from the curated CTD Gene-Disease Associations dataset.
Musculoskeletal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Musculoskeletal Diseases from the curated CTD Gene-Disease Associations dataset.
Ear Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ear Diseases from the curated CTD Gene-Disease Associations dataset.
Genital Diseases, Female Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Female from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

down syndrome; fetal diseases Gene Set

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set

down syndrome; ehlers-danlos syndrome Gene Set

gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set

bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma Gene Set

alcoholic liver diseases; alcoholism; liver diseases; liver diseases, alcoholic Gene Set

cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene Set

abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

Transient Myeloproliferative Disorder of Down Syndrome Gene Set

Leukemia, Megakaryoblastic, of Down Syndrome Gene Set

Down Syndrome Gene Set

down syndrome Gene Set

down syndrome; hirschsprung disease; nondisjunction, genetic Gene Set

alzheimer disease; down syndrome Gene Set

down syndrome; nondisjunction, genetic Gene Set

down syndrome; trisomy Gene Set

down syndrome; leukemia, myeloid; myeloid leukemia Gene Set

down syndrome; hepatitis b; hypothyroidism Gene Set

down syndrome; micronuclei, chromosome-defective Gene Set

down syndrome; leukemia, myeloid, acute Gene Set

dementia; down syndrome Gene Set

down syndrome; heart defects, congenital Gene Set

alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set

down syndrome Gene Set

down syndrome; precursor cell lymphoblastic leukemia-lymphoma Gene Set

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

alzheimer's disease; down syndrome Gene Set

down's syndrome Gene Set

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

down syndrome; Gene Set

alzheimer disease; down syndrome; Gene Set

celiac disease; down syndrome Gene Set

Down Syndrome Gene Set

leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set

down syndrome Gene Set

leukemia, transient, of down syndrome Gene Set

Down syndrome Gene Set

Down Syndrome Gene Set

Down Syndrome Critical Region Gene Set

Myeloid Leukemia Associated With Down Syndrome Gene Set

Transient Myeloproliferative Disorder Of Down Syndrome Gene Set

Myeloid Proliferations Associated With Down Syndrome Gene Set

Down syndrome Gene Set

Down syndrome Gene Set

Myeloid leukemia associated with Down Syndrome Gene Set

Down syndrome Gene Set

Acute megakaryoblastic leukemia in down syndrome Gene Set

genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene Set

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic; rheumatic diseases; rheumatism; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set

autoimmune diseases; liver diseases; syndrome Gene Set

Fetal Diseases Gene Set

fetal diseases; hemoglobinopathies Gene Set

fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set

diabetes mellitus, type 2; fetal diseases; malnutrition; starvation Gene Set

fetal diseases; hemophilia a Gene Set

beta thalassemia; beta-thalassemia; fetal diseases Gene Set

fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene Set

fetal growth retardation; periodontal diseases; pregnancy complications Gene Set

alpha thalassemia; alpha-thalassemia; fetal diseases Gene Set

fetal diseases; infection Gene Set

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set

Fetal Diseases Gene Set

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway Gene Set

down Gene Set

Down Syndrome_CNS - Brain - Cerebellum (MMHCC)_GSE1611 Gene Set

Down Syndrome_Brain_GSE5390 Gene Set

Down Syndrome_Fetus_GSE10758 Gene Set