Hypothalamic Dysfunction Syndromes

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Results for "Hypothalamic Dysfunction Syndromes": 445 gene sets

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Hypothalamic Dysfunction Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Dysfunction Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic-Pituitary-Adrenal Axis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic-Pituitary-Adrenal Axis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventromedial hypothalamic nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventromedial hypothalamic nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior region, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, mammillary region, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, mammillary region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior region, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
dorsomedial hypothalamic nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in dorsomedial hypothalamic nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior hypothalamic area, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, tuberal region, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, tuberal region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
posterior hypothalamic area, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
posterior hypothalamic area, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, mammillary region, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, mammillary region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
ventromedial hypothalamic nucleus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventromedial hypothalamic nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
anterior hypothalamic area, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, descending division, lateral parvicellular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, descending division, lateral parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Arcuate hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Arcuate hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, magnocellular division, medial magnocellular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division, medial magnocellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, parvicellular division, medial parvicellular part, dorsal zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division, medial parvicellular part, dorsal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Periventricular hypothalamic nucleus, posterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Periventricular hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
hypothalamic amygdala Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in hypothalamic amygdala relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lower dorsal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lower dorsal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Hypothalamic medial zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Hypothalamic medial zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper dorsal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper dorsal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part, lateral zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part, lateral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, parvicellular division Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
preopto-hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in preopto-hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, dorsomedial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
peduncular part of dorsomedial hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in peduncular part of dorsomedial hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Hypothalamic lateral zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Hypothalamic lateral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
preopto-hypothalamic band Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in preopto-hypothalamic band relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lower basal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lower basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, posterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, magnocellular division Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Paraventricular hypothalamic nucleus, descending division Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, descending division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, ventrolateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, ventrolateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posterior part of anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior part of anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lateral anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
magnocellular superficial hypothalamic nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in magnocellular superficial hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, anterior part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper basal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior hypothalamic nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, tuberal part Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, tuberal part relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
ventromedial hypothalamic nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventromedial hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in hypothalamic portion Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in hypothalamic portion relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
lateral hypothalamic area, anterior part Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral hypothalamic area, anterior part relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
dorsomedial hypothalamic nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in dorsomedial hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
posterior hypothalamic nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Hypothalamic hamartomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothalamic hamartomas from the curated CTD Gene-Disease Associations dataset.
hypothalamic neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypothalamic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypothalamic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypothalamic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amenorrhea; hypogonadism; hypothalamic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease amenorrhea; hypogonadism; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypothalamic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hypothalamic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
hypothalamic tangential migration using cell-axon interactions Gene Set From GO Biological Process Annotations 2015 genes participating in the hypothalamic tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations 2015 dataset.
hypothalamic gonadotropin-releasing hormone (gnrh) deficiency Gene Set From HPO Gene-Disease Associations genes associated with the hypothalamic gonadotropin-releasing hormone (gnrh) deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypothalamic hypothyroidism Gene Set From HPO Gene-Disease Associations genes associated with the hypothalamic hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypothalamic hamartoma Gene Set From HPO Gene-Disease Associations genes associated with the hypothalamic hamartoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal paraventricular hypothalamic nucleus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal paraventricular hypothalamic nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{hypothalamic hamartomas, somatic} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypothalamic hamartomas, somatic} phenotype from the curated OMIM Gene-Disease Associations dataset.
posterior hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
ventromedial hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ventromedial hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
dorsal hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue dorsal hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
anterior hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue anterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Hypothalamic Hamartomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Obesity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Amenorrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Amenorrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Gonadotropin-Releasing Hormone Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypothalamic Gonadotropin-Releasing Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypothalamic Luteinizing Hormone-Releasing Hormone Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypothalamic Luteinizing Hormone-Releasing Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
hypothalamic tangential migration using cell-axon interactions Gene Set From GO Biological Process Annotations 2023 genes participating in the hypothalamic tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased ventromedial hypothalamic nucleus size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ventromedial hypothalamic nucleus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ventromedial hypothalamic nucleus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ventromedial hypothalamic nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal paraventricular hypothalamic nucleus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal paraventricular hypothalamic nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Extra-SCN hypothalamic neuron_Eye_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Extra-SCN hypothalamic neuron_Eye_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
hypothalamic tangential migration using cell-axon interactions Gene Set From GO Biological Process Annotations 2025 genes participating in the hypothalamic tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations 2025 dataset.
Hypothalamic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypothalamic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypothalamic neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypothalamic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Ventromedial hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ventromedial hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Anterior hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Posterior hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Dorsal hypothalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Dorsal hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hypothalamic hypothyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypothalamic hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary Paraganglioma-Pheochromocytoma Syndromes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paraganglioma-Pheochromocytoma Syndromes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Usher Syndromes from the curated CTD Gene-Disease Associations dataset.
Trichothiodystrophy Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichothiodystrophy Syndromes from the curated CTD Gene-Disease Associations dataset.
Neurotoxicity Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurotoxicity Syndromes from the curated CTD Gene-Disease Associations dataset.
Sleep Apnea Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea Syndromes from the curated CTD Gene-Disease Associations dataset.
Myelodysplastic Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myelodysplastic Syndromes from the curated CTD Gene-Disease Associations dataset.
Malabsorption Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Malabsorption Syndromes from the curated CTD Gene-Disease Associations dataset.
Dry Eye Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dry Eye Syndromes from the curated CTD Gene-Disease Associations dataset.
Orofaciodigital Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orofaciodigital Syndromes from the curated CTD Gene-Disease Associations dataset.
Cryopyrin-Associated Periodic Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cryopyrin-Associated Periodic Syndromes from the curated CTD Gene-Disease Associations dataset.
Myasthenic Syndromes, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic Syndromes, Congenital from the curated CTD Gene-Disease Associations dataset.
Bone Marrow failure syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Marrow failure syndromes from the curated CTD Gene-Disease Associations dataset.
Compartment Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Compartment Syndromes from the curated CTD Gene-Disease Associations dataset.
Immunologic Deficiency Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunologic Deficiency Syndromes from the curated CTD Gene-Disease Associations dataset.
non-st-elevation acute coronary syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease non-st-elevation acute coronary syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
usher syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease usher syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary syndromes, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary syndromes, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage; dna damage; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage; dna damage; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; fragile x syndromes; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; fragile x syndromes; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; fragile x syndromes; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; fragile x syndromes; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, pre-b-cell; neurotoxicity syndromes; precursor b-cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, pre-b-cell; neurotoxicity syndromes; precursor b-cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchiectasis; immunologic deficiency syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchiectasis; immunologic deficiency syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dry eye syndromes; Gene Set From GAD Gene-Disease Associations genes associated with the disease dry eye syndromes; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complex regional pain syndromes; dystonia; Gene Set From GAD Gene-Disease Associations genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; corneal diseases; dry eye syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; corneal diseases; dry eye syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurotoxicity syndromes; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease neurotoxicity syndromes; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelomonocytic, chronic; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurotoxicity syndromes; pancreatic neoplasm; pancreatic neoplasms; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease neurotoxicity syndromes; pancreatic neoplasm; pancreatic neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; fragile x syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; parkinson disease; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; parkinson disease; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prader-willi and angelman syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease prader-willi and angelman syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; neurotoxicity syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia; fragile x syndrome; fragile x syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia; fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; myeloproliferative disorders; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; myeloproliferative disorders; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
immunologic deficiency syndromes; severe combined immunodeficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease immunologic deficiency syndromes; severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
syndromes Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term syndromes in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Neurotoxicity Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neurotoxicity Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myelodysplastic Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myelodysplastic Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paraneoplastic Syndromes, Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paraneoplastic Syndromes, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Usher Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Usher Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cryopyrin-associated Periodic Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cryopyrin-associated Periodic Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Complex Regional Pain Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Complex Regional Pain Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neoplastic Syndromes, Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplastic Syndromes, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Immunologic Deficiency Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Immunologic Deficiency Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dry Eye Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dry Eye Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurocutaneous Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurocutaneous Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epileptic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epileptic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complex Regional Pain Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complex Regional Pain Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myasthenic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myasthenic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microdeletion Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microdeletion Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bone Marrow Failure Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bone Marrow Failure Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryopyrin-Associated Periodic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryopyrin-Associated Periodic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Euthyroid Sick Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Euthyroid Sick Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Instability Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Instability Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
De Novo Myelodysplastic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease De Novo Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myofascial Pain Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myofascial Pain Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trichothiodystrophy Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trichothiodystrophy Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Myelodysplastic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Syndromes, Ocular Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Syndromes, Ocular in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Congenital Malformation Syndromes With Other Skeletal Changes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformation Syndromes With Other Skeletal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Deaf-Blind Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Deaf-Blind Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synaptic congenital myasthenic syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Synaptic congenital myasthenic syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PTEN hamartoma tumor syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PTEN hamartoma tumor syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Human HOXA1 syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Human HOXA1 syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN9A-related neuropathic pain syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN9A-related neuropathic pain syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-del(5q) myelodysplastic syndromes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-del(5q) myelodysplastic syndromes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ticagrelor levels in individuals with acute coronary syndromes treated with ticagrelor Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ticagrelor levels in individuals with acute coronary syndromes treated with ticagrelor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensorineural deafness with mild renal dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction from the curated CTD Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phagocyte Bactericidal Dysfunction from the curated CTD Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Dysfunction Syndrome from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Left Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset.
Sexual Dysfunction, Physiological Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sexual Dysfunction, Physiological from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erectile Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Right Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis renal dysfunction cholestasis syndrome from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset.
Sphincter of Oddi Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sphincter of Oddi Dysfunction from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Erectile Dysfunction in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ovarian dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ovarian dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
physiological sexual disorders; sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease physiological sexual disorders; sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; inflammation; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; inflammation; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
biliary atresia; liver diseases; primary graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; erectile dysfunction; hypogonadism Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; erectile dysfunction; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endothelial dysfunction in normal humans. Gene Set From GAD Gene-Disease Associations genes associated with the disease endothelial dysfunction in normal humans. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
left ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease left ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; autonomic nervous system dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; autonomic nervous system dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis-related organ dysfunction and shock after burn injury Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis-related organ dysfunction and shock after burn injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary vascular endothelial dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary vascular endothelial dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; coronary endothelial vasomotor dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; coronary endothelial vasomotor dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; renal dysfunction, posttransplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; renal dysfunction, posttransplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; myocardial dysfunction, non-ischaemic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; myocardial dysfunction, non-ischaemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dysfunction Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dysfunction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sexual dysfunction Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sexual dysfunction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
autonomic bladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic bladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
beta-cell dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the beta-cell dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vestibular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the vestibular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gallbladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the gallbladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autonomic erectile dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic erectile dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
urinary bladder sphincter dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the urinary bladder sphincter dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal tubular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the renal tubular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
orthostatic hypotension due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ventricular Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Posterior Tibial Tendon Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Left Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Left phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Graft Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sexual Dysfunction, Physiological Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sexual Dysfunction, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Right Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
multisystemic smooth muscle dysfunction syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the multisystemic smooth muscle dysfunction syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set From OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
autonomic nervous system dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the autonomic nervous system dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
sinoatrial node dysfunction and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the sinoatrial node dysfunction and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.
sensorineural deafness with mild renal dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
Surfactant Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Metabolism Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysfunction Adrenal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysfunction Adrenal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Microvascular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Microvascular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Memory Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Memory Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculogenic Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculogenic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Diastolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Placental Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bowel Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bowel Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minimal Brain Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minimal Brain Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organ Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organ Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Deficiency Or Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Deficiency Or Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinus Node Dysfunction (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinus Node Dysfunction (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Executive Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Executive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meibomian Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meibomian Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutrophil Actin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutrophil Actin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symphysis Pubis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symphysis Pubis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autonomic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Female Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorineural Deafness With Mild Renal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pangastrointestinal System Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pangastrointestinal System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinoatrial Node Dysfunction And Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinoatrial Node Dysfunction And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colonic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Colonic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emotional Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emotional Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phagocyte Bactericidal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Male Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Male Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Segmental Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Segmental Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pineal Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pineal Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Tibial Tendon Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyramidal Tract Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Tract Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonneurogenic Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonneurogenic Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroxisomal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Dysfunction With T-Cell Inactivation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Dysfunction With T-Cell Inactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Dysfunction, Postpartum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Dysfunction, Postpartum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Myocardial Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Myocardial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endothelial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endothelial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Liver Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Liver Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Beta-Cell Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beta-Cell Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Urinary Bladder Sphincter Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Urinary Bladder Sphincter Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postoperative Cognitive Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Cognitive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysfunction Of Lateral Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysfunction Of Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurologic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurologic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Orthostatic Hypotension Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vestibular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vestibular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gastrointestinal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Uterine Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uterine Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Erectile Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Right Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Nervous System Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Nervous System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Abnormality Related To Mitochondrial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Abnormality Related To Mitochondrial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Speech Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Speech Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Primary Graft Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Sweating Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diastolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence Gene Set From WikiPathways Pathways 2024 proteins participating in the NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence pathway from the WikiPathways Pathways 2024 dataset.
SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
ROS in COVID 19 endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the ROS in COVID 19 endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Metabolic dysfunction-associated steatotic liver disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ovarian dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Metabolic dysfunction-associated steatotic liver disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovarian dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction and alcohol associated liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatotic liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatohepatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatohepatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thiamine metabolism dysfunction syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine metabolism dysfunction syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Surfactant metabolism dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Surfactant metabolism dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multisystemic smooth muscle dysfunction syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multisystemic smooth muscle dysfunction syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary Surfactant Metabolism Dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary Surfactant Metabolism Dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diastolic dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diastolic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine Metabolism Dysfunction Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine Metabolism Dysfunction Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Memory dysfunction in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Memory dysfunction in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Hypothalamic Dysfunction Syndromes Gene Set

Hypothalamic-Pituitary-Adrenal Axis Dysfunction Gene Set

myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set

ventromedial hypothalamic nucleus, left Gene Set

lateral hypothalamic area, anterior region, left Gene Set

lateral hypothalamic area, mammillary region, right Gene Set

lateral hypothalamic area, anterior region, right Gene Set

dorsomedial hypothalamic nucleus, left Gene Set

anterior hypothalamic area, right Gene Set

lateral hypothalamic area, tuberal region, left Gene Set

posterior hypothalamic area, left Gene Set

posterior hypothalamic area, right Gene Set

lateral hypothalamic area, mammillary region, left Gene Set

ventromedial hypothalamic nucleus, right Gene Set

anterior hypothalamic area, left Gene Set

Paraventricular hypothalamic nucleus, descending division, lateral parvicellular part Gene Set

Ventromedial hypothalamic nucleus Gene Set

Arcuate hypothalamic nucleus Gene Set

Lateral hypothalamic area Gene Set

Paraventricular hypothalamic nucleus, magnocellular division, medial magnocellular part Gene Set

Anterior hypothalamic nucleus, central part Gene Set

Posterior hypothalamic nucleus Gene Set

Paraventricular hypothalamic nucleus, parvicellular division, medial parvicellular part, dorsal zone Gene Set

Paraventricular hypothalamic nucleus Gene Set

Periventricular hypothalamic nucleus, posterior part Gene Set

hypothalamic amygdala Gene Set

lower dorsal lateral hypothalamic area Gene Set

Hypothalamic medial zone Gene Set

upper dorsal lateral hypothalamic area Gene Set

Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part, lateral zone Gene Set

Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part Gene Set

Paraventricular hypothalamic nucleus, parvicellular division Gene Set

preopto-hypothalamic area Gene Set

Ventromedial hypothalamic nucleus, dorsomedial part Gene Set

peduncular part of dorsomedial hypothalamic nucleus Gene Set

Ventromedial hypothalamic nucleus, central part Gene Set

Hypothalamic lateral zone Gene Set

preopto-hypothalamic band Gene Set

Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part Gene Set

Anterior hypothalamic nucleus Gene Set

lower basal lateral hypothalamic area Gene Set

Anterior hypothalamic nucleus, posterior part Gene Set

Paraventricular hypothalamic nucleus, magnocellular division Gene Set

Paraventricular hypothalamic nucleus, descending division Gene Set

Ventromedial hypothalamic nucleus, ventrolateral part Gene Set

posterior part of anterior hypothalamic nucleus Gene Set

lateral anterior hypothalamic nucleus Gene Set

Ventromedial hypothalamic nucleus, anterior part Gene Set

magnocellular superficial hypothalamic nucleus Gene Set

Anterior hypothalamic nucleus, anterior part Gene Set

upper basal lateral hypothalamic area Gene Set

anterior hypothalamic nucleus Gene Set

lateral hypothalamic area, tuberal part Gene Set

ventromedial hypothalamic nucleus Gene Set

VZ in hypothalamic portion Gene Set

lateral hypothalamic area, anterior part Gene Set

dorsomedial hypothalamic nucleus Gene Set

posterior hypothalamic nucleus Gene Set

Hypothalamic hamartomas Gene Set

hypothalamic neoplasm Gene Set

hypothalamic disease Gene Set

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

amenorrhea; hypogonadism; hypothalamic diseases Gene Set

hypothalamic Gene Set

hypothalamic tangential migration using cell-axon interactions Gene Set

hypothalamic gonadotropin-releasing hormone (gnrh) deficiency Gene Set

hypothalamic hypothyroidism Gene Set

hypothalamic hamartoma Gene Set

abnormal paraventricular hypothalamic nucleus morphology Gene Set

{hypothalamic hamartomas, somatic} Gene Set

posterior hypothalamic nucleus Gene Set

ventromedial hypothalamic nucleus Gene Set

hypothalamic nucleus Gene Set

dorsal hypothalamic nucleus Gene Set

anterior hypothalamic nucleus Gene Set

Hypothalamic Hamartomas Gene Set

Hypothalamic Diabetes Insipidus Gene Set

Hypothalamic Obesity Gene Set

Hypothalamic Amenorrhea Gene Set