Idiopathic Infantile Hypercalcemia

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Results for "Idiopathic Infantile Hypercalcemia - Mild Form": 717 gene sets

Name
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic hypercalcemia of infancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic hypercalcemia of infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
infantile hypercalcemia Gene Set From HPO Gene-Disease Associations genes associated with the infantile hypercalcemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypercalcemia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypercalcemia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.
Infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic fibrosing alveolitis, chronic form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic fibrosing alveolitis, chronic form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
juvenile polyposis syndrome, infantile form Gene Set From OMIM Gene-Disease Associations genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset.
Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypercalciuric hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercalciuric hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercalcemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercalcemia from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.
hypercalcemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypercalcemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic renal failure; hypercalcemia; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypercalcemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercalcemia; hyperparathyroidism, primary Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercalcemia; hyperparathyroidism, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercalcemia; hypercalciuria Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercalcemia; hypercalciuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercalcemia; sarcoidosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercalcemia; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypocalciuric hypercalcemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercalcemia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hypercalcemia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
hypercalcemia Gene Set From HPO Gene-Disease Associations genes associated with the hypercalcemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hypercalcemia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypercalcemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hypercalciuric hypercalcemia Gene Set From OMIM Gene-Disease Associations genes associated with the hypercalciuric hypercalcemia phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalciuric hypercalcemia, type i Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, type i phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalciuric hypercalcemia, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalciuric hypercalcemia, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
humoral hypercalcemia of malignancy Gene Set From OMIM Gene-Disease Associations genes associated with the humoral hypercalcemia of malignancy phenotype from the curated OMIM Gene-Disease Associations dataset.
Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Humoral Hypercalcemia Of Malignancy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Humoral Hypercalcemia Of Malignancy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocalciuric Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocalciuric Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocalciuric Hypercalcemia, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocalciuric Hypercalcemia, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercalcemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypercalcemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypercalcemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypocalciuric hypercalcemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hypocalciuric hypercalcemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypocalciuric hypercalcemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hypocalciuric hypercalcemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypocalciuric hypercalcemia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hypocalciuric hypercalcemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypocalciuric hypercalcemia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hypocalciuric hypercalcemia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypocalciuric hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hypocalciuric hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta with normal sclerae, dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta with normal sclerae, dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal recessive form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vohwinkel Syndrome, Variant Form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vohwinkel Syndrome, Variant Form from the curated CTD Gene-Disease Associations dataset.
Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.
Hepatorenal form of glycogen storage disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset.
Ehlers-Danlos syndrome, cardiac valvular form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos syndrome, cardiac valvular form from the curated CTD Gene-Disease Associations dataset.
Ehlers-Danlos syndrome, progeroid form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos syndrome, progeroid form from the curated CTD Gene-Disease Associations dataset.
form agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease form agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
1,6-Fructose Diphosphate (Linear Form) Gene Set From DrugBank Drug Targets interacting proteins for the 1,6-Fructose Diphosphate (Linear Form) drug from the curated DrugBank Drug Targets dataset.
immunologically hyper-reactive form of onchocerciasis (sowda) Gene Set From GAD Gene-Disease Associations genes associated with the disease immunologically hyper-reactive form of onchocerciasis (sowda) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyper-igm syndrome can form oligomers and trigger cd40-mediated signals Gene Set From GAD Gene-Disease Associations genes associated with the disease hyper-igm syndrome can form oligomers and trigger cd40-mediated signals in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
form Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term form in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
y-form dna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the y-form dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
latanoprost (free acid form) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the latanoprost (free acid form) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
misoprostol (free acid form) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the misoprostol (free acid form) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
butaprost (free acid form) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the butaprost (free acid form) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
bimatoprost (free acid form) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the bimatoprost (free acid form) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
abnormal form of the vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
PLUNC, long form Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PLUNC, long form protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Phenylalanine-4-hydroxylase, tetrameric form Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Phenylalanine-4-hydroxylase, tetrameric form protein domain from the InterPro Predicted Protein Domain Annotations dataset.
failure to form blastocele Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure to form blastocele phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure to form egg cylinders Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure to form egg cylinders phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ehlers-danlos syndrome, cardiac valvular form Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, cardiac valvular form phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body disease, adult form Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body disease, adult form phenotype from the curated OMIM Gene-Disease Associations dataset.
organism form Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue organism form from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
plant form Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue plant form from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
organism form Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue organism form in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
plant form Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue plant form in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
procyclic form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue procyclic form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bloodstream form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bloodstream form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
metacyclic form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue metacyclic form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
fungus form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fungus form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
trypanosomoid form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue trypanosomoid form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
organism form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue organism form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
plant form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue plant form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
sporozoan form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue sporozoan form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
protozoan form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue protozoan form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Hepatic Form Of Wilson Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Form Of Wilson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Active Ebv Infection Of T-And Nk-Cell Type, Systemic Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Active Ebv Infection Of T-And Nk-Cell Type, Systemic Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zoonotic Form Of Cutaneous Leishmaniasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zoonotic Form Of Cutaneous Leishmaniasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gsd Iv, Neumuscular Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gsd Iv, Neumuscular Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Disease, Adult Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Disease, Adult Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hunter'S Syndrome, Severe Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hunter'S Syndrome, Severe Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acropectorovertebral Dysplasia, F-Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acropectorovertebral Dysplasia, F-Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vohwinkel Syndrome, Variant Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vohwinkel Syndrome, Variant Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Form Of Celiac Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Form Of Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Form Of The Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Form Of The Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impaired Ability To Form Peer Relationships Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Ability To Form Peer Relationships in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
peptidyl-histidine methylation, to form tele-methylhistidine Gene Set From GO Biological Process Annotations 2023 genes participating in the peptidyl-histidine methylation, to form tele-methylhistidine biological process from the curated GO Biological Process Annotations 2023 dataset.
Y-form DNA binding Gene Set From GO Molecular Function Annotations 2023 genes performing the Y-form DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
Y-form DNA binding Gene Set From GO Molecular Function Annotations 2025 genes performing the Y-form DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Form agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Form agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Organism form Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Organism form from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Organism form Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Organism form in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Organism form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Organism form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Trypanosomoid form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Trypanosomoid form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Sporozoan form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Sporozoan form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Plant form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Plant form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Protozoan form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Protozoan form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bloodstream form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bloodstream form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Procyclic form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Procyclic form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Metacyclic form Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Metacyclic form in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
yeast-form cell wall Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the yeast-form cell wall cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Autosomal dominant optic atrophy classic form Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant optic atrophy classic form phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disease progression to geographic atrophy form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to geographic atrophy form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to choroidal neovascularization form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to choroidal neovascularization form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
INDOCYANINE GREEN ACID FORM Gene Set From DGIdb Drug Targets 2026 interacting proteins for the INDOCYANINE GREEN ACID FORM drug from theDGIdb Drug Targets 2026 dataset.
BUTAPROST (FREE ACID FORM) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the BUTAPROST (FREE ACID FORM) drug from theDGIdb Drug Targets 2026 dataset.
BIMATOPROST (FREE ACID FORM) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the BIMATOPROST (FREE ACID FORM) drug from theDGIdb Drug Targets 2026 dataset.
LATANOPROST (FREE ACID FORM) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the LATANOPROST (FREE ACID FORM) drug from theDGIdb Drug Targets 2026 dataset.
TUMOUR NECROSIS FACTOR MEMBRANE FORM Gene Set From DGIdb Drug Targets 2026 interacting proteins for the TUMOUR NECROSIS FACTOR MEMBRANE FORM drug from theDGIdb Drug Targets 2026 dataset.
TUMOUR NECROSIS FACTOR SHED FORM Gene Set From DGIdb Drug Targets 2026 interacting proteins for the TUMOUR NECROSIS FACTOR SHED FORM drug from theDGIdb Drug Targets 2026 dataset.
Short stature, idiopathic, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutropenia, nonimmune chronic idiopathic, of adults Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Basal ganglia calcification, idiopathic, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia calcification, idiopathic, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, idiopathic, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.
Idiopathic dilation cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic dilation cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Purpura, Thrombocytopenic, Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura, Thrombocytopenic, Idiopathic from the curated CTD Gene-Disease Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrotic syndrome, idiopathic, steroid-resistant from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic basal ganglia calcification 1 from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Nonimmune Chronic Idiopathic, Adult Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Nonimmune Chronic Idiopathic, Adult from the curated CTD Gene-Disease Associations dataset.
Jaundice, Chronic Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Chronic Idiopathic from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Hypogonadotropic Hypogonadism from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic interstitial pneumonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic cd4-positive t-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic cd4-positive t-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
systemic juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease systemic juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriage. Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic thrombotic thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic thrombotic thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic premature ovarian failure Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriages Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic infertility Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic deep venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic deep venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonfamilial idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nonfamilial idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic short stature Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic atrial fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic atrial fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic environmental intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic environmental intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypersomnolence, idiopathic; narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypersomnolence, idiopathic; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, idiopathic dilated Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, idiopathic dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic idiopathic neutropenia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic idiopathic neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis (juvenile idiopathic) Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis (juvenile idiopathic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic chronic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic chronic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic orthostatic intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic orthostatic intolerance 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.
h. pylori infection; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent or chronic idiopathic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic torsion dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, idiopathic thrombocytopenic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, idiopathic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood idiopathic thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema Gene Set From GAD Gene-Disease Associations genes associated with the disease graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic; werlhof's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic; werlhof's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic azoospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic azoospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy, idiopathic inflammatory Gene Set From GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter infections; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter infections; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term idiopathic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Nephropathy (idiopathic membranous) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Nephropathy (idiopathic membranous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
idiopathic interstitial pneumonia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic interstitial pneumonia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypersomnolence, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Purpura, Thrombocytopenic, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Thrombocytopenic, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Interstitial Pneumonias phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hyperostosis, Diffuse Idiopathic Skeletal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperostosis, Diffuse Idiopathic Skeletal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, nonimmune chronic idiopathic, of adults Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary fibrosis, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypereosinophilic syndrome, idiopathic, resistant to imatinib Gene Set From OMIM Gene-Disease Associations genes associated with the hypereosinophilic syndrome, idiopathic, resistant to imatinib phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary fibrosis, idiopathic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
hydrocephalus with congenital idiopathic intestinal pseudoobstruction Gene Set From OMIM Gene-Disease Associations genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{pancreatitis, idiopathic} Gene Set From OMIM Gene-Disease Associations genes associated with the {pancreatitis, idiopathic} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Achalasia Of Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Achalasia Of Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Inflammatory Myopathies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Inflammatory Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Bronchiectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Arterial Calcification Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Arterial Calcification Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypereosinophilic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypereosinophilic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Crescentic Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Crescentic Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Urticaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Normal Pressure Hydrocephalus (Inph) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Normal Pressure Hydrocephalus (Inph) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Premature Ovarian Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Premature Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Membranous Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pneumonia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pneumonia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trigeminal Neuralgia, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trigeminal Neuralgia, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypoparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Chronic Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Focal Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Focal Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Torsion Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Torsion Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Central Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Interstitial Pneumonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
(Idiopathic) Normal Pressure Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease (Idiopathic) Normal Pressure Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unspecified Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unspecified Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Transverse Myelitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Transverse Myelitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile And Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile And Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Polypoidal Choroidal Vasculopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Polypoidal Choroidal Vasculopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Urethral Stricture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Urethral Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
T-Lymphocytopenia, Idiopathic Cd4-Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease T-Lymphocytopenia, Idiopathic Cd4-Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Copper Toxicosis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Copper Toxicosis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Myositis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Myositis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Retroperitoneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Retroperitoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Uveitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Uveitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercatabolic Hypoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercatabolic Hypoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnolence, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia (Itp) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia (Itp) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Gynecomastia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Gynecomastia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Juxtafoveal Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Juxtafoveal Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Granulomatous Mastitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Granulomatous Mastitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Growth Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymyositis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymyositis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Basal Ganglia Calcification 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Basal Ganglia Calcification 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Atrophoderma Of Pasini And Pierini Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Atrophoderma Of Pasini And Pierini in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Idiopathic Intestinal Pseudoobstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Idiopathic Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature, Idiopathic, Autosomal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Extrahepatic Biliary Atresia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypopituitarism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypopituitarism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Cirrhotic Portal Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Cirrhotic Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Diabetes (Mellitus) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Diabetes (Mellitus) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extended Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extended Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Recurrent Pericarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Acute Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Acute Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cd4 Lymphocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cd4 Lymphocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Anaphylaxis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Anaphylaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Angioedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cardiac Hypertrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cardiac Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary And Idiopathic Neuropathy, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary And Idiopathic Neuropathy, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psoriatic Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psoriatic Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Guttate Hypomelanosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Guttate Hypomelanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Multicentric Osteolyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Multicentric Osteolyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypertrophic Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypertrophic Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hyperprolactinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hyperprolactinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Autoimmune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Autoimmune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parkinsonism Or Parkinson'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parkinsonism Or Parkinson'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Membranous Glomerulopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic Hirsutism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Idiopathic Hirsutism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chronic Idiopathic Constipation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Idiopathic Constipation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic pulmonary fibrosis cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) pathway from the Reactome Pathways 2024 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic scoliosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic scoliosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic peripheral autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic peripheral autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic CD4-positive T-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic CD4-positive T-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic pulmonary fibrosis disease specific cell type Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Idiopathic pulmonary fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic steroid-resistant nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic and/or familial pulmonary arterial hypertension Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic and/or familial pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic Pulmonary Fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic basal ganglia calcification Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic basal ganglia calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic hypereosinophilic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic hypereosinophilic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic camptocormia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic camptocormia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic CD4 lymphocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic CD4 lymphocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonimmune chronic idiopathic neutropenia of adults Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonimmune chronic idiopathic neutropenia of adults phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic hypercalciuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic hypercalciuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic scoliosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic environmental intolerance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic environmental intolerance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic inflammatory myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Systemic juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic osteonecrosis of the femoral head Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic downbeat nystagmus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic downbeat nystagmus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic inflammatory myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic membranous nephropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic membranous nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic intracranial hypertension Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic intracranial hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (oligoarticular juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (oligoarticular juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation with infantile enterocolitis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation with infantile enterocolitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Galactosialidosis, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine palmitoyltransferase II deficiency, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type II, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked infantile nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile myofibromatosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile myofibromatosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amish infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Galactosialidosis, early infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyloric stenosis, infantile hypertrophic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Metachromatic leukodystrophy, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metachromatic leukodystrophy, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal neurodegeneration with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal neurodegeneration with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease, infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Liver failure acute infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Liver failure acute infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sting-associated vasculopathy, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sialic acid storage disease, severe infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune disease, multisystem, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinsonism-Dystonia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Hereditary spastic paralysis, infantile onset ascending Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.
Ceroid lipofuscinosis, neuronal 1, infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.
Infantile polyarteritis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infantile polyarteritis from the curated CTD Gene-Disease Associations dataset.
LIVER FAILURE, INFANTILE, TRANSIENT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LIVER FAILURE, INFANTILE, TRANSIENT from the curated CTD Gene-Disease Associations dataset.
Refsum Disease, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.
Glaucoma 3, primary infantile, B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amish Infantile Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.
Hemangioma, capillary infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemangioma, capillary infantile from the curated CTD Gene-Disease Associations dataset.
Striatonigral degeneration infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 5 from the curated CTD Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spasms, Infantile from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.
Hypophosphatasia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Infantile from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
infantile refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal infantile encephalocardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal infantile encephalocardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neurofibromatosis 1; spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease neurofibromatosis 1; spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypophosphatasia Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypophosphatasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variant late infantile neuronal ceroid lipofuscinosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile-onset ascending hereditary spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term infantile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
calcific stippling of infantile cartilaginous skeleton Gene Set From HPO Gene-Disease Associations genes associated with the calcific stippling of infantile cartilaginous skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile onset Gene Set From HPO Gene-Disease Associations genes associated with the infantile onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile spasms Gene Set From HPO Gene-Disease Associations genes associated with the infantile spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile axial hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile axial hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spasms, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infantile Apparent Life-Threatening Event Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infantile Apparent Life-Threatening Event phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Diarrhea, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Diarrhea, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
pyloric stenosis, infantile hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 24 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 25 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 26 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 23 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
amish infantile epilepsy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the amish infantile epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertriglyceridemia, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypertriglyceridemia, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
liver failure, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the liver failure, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
?myofibromatosis, infantile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?myofibromatosis, infantile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
nephronophthisis 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the nephronophthisis 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myofibromatosis, infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myofibromatosis, infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuroaxonal neurodegeneration, infantile, with facial dysmophism Gene Set From OMIM Gene-Disease Associations genes associated with the neuroaxonal neurodegeneration, infantile, with facial dysmophism phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinsonism-dystonia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
sting-associated vasculopathy, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
{hemangioma, capillary infantile, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hemangioma, capillary infantile, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus, infantile periodic alternating, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
hemangioma, capillary infantile, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the hemangioma, capillary infantile, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, infantile, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
?epileptic encephalopathy, early infantile, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set From OMIM Gene-Disease Associations genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypophosphatasia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatasia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
sandhoff disease, infantile, juvenile, and adult forms Gene Set From OMIM Gene-Disease Associations genes associated with the sandhoff disease, infantile, juvenile, and adult forms phenotype from the curated OMIM Gene-Disease Associations dataset.
sialic acid storage disorder, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the sialic acid storage disorder, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
autoinflammation with infantile enterocolitis Gene Set From OMIM Gene-Disease Associations genes associated with the autoinflammation with infantile enterocolitis phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune disease, multisystem, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set From OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.
striatonigral degeneration, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
glaucoma 3, primary infantile, b Gene Set From OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary infantile, b phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paralysis, infantile onset ascending Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.
Infantile Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Spasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Spasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Nystagmus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Nystagmus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Myofibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Myofibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Infantile Neuronal Ceroid Lipfuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Infantile Neuronal Ceroid Lipfuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Severe Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Severe Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Scurvy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Scurvy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Infantile Neurological, Cutaneous, And Articular Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy With Suppression Bursts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy With Suppression Bursts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hypophosphatasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hypophosphatasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemangioma, Capillary Infantile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemangioma, Capillary Infantile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration, Infantile, Mitochondrial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration, Infantile, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Malignant Osteopetrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Malignant Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endemic Tyrolean Infantile Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Endemic Tyrolean Infantile Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amish Infantile Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Encephalopathy, Infantile Subacute, Of Leigh in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Infantile Nystagmus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Refsum Disease (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Refsum Disease (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Infantile Myasthenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Onset Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Onset Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystinosis, Infantile Nephropathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystinosis, Infantile Nephropathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fastkd2-Related Infantile Mitochondrial Encephalomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fastkd2-Related Infantile Mitochondrial Encephalomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Atopic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Globoid Cell Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Globoid Cell Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sandhoff Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sandhoff Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sting-Associated Vasculopathy, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sting-Associated Vasculopathy, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Digital Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Digital Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Liver Failure Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Liver Failure Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Constant Exotropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Constant Exotropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gm 2 Gangliosidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gm 2 Gangliosidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Infantile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Infantile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monoplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monoplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gastroenteritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Infantile Mitochondrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Infantile Mitochondrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Free Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Free Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma And Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma And Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver Failure, Infantile, Transient Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver Failure, Infantile, Transient in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Diarrhea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Nystagmus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Obesity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Axial Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Axial Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hemangioma, Capillary Infantile, Somatic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hemangioma, Capillary Infantile, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Colic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Colic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 pathway from the Reactome Pathways 2024 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 pathway from the Reactome Pathways 2024 dataset.
COX deficiency, infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early infantile epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early infantile epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile Refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile Refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile parkinsonism-dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile parkinsonism-dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypophosphatasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile myofibromatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile myofibromatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient infantile liver failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient infantile liver failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypotonia with psychomotor retardation and characteristic facies-3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypotonia with psychomotor retardation and characteristic facies-3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile histiocytoid cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile histiocytoid cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-infantile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-infantile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic infantile neurological Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic infantile neurological phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile onset spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile onset spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal/infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal/infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Capillary infantile hemangioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary infantile hemangioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign sporadic infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign sporadic infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LAMB2-related infantile-onset nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LAMB2-related infantile-onset nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephropathic cystinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephropathic cystinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile spasms Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile spasms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile convulsions and choreoathetosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile convulsions and choreoathetosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile myofibromatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile myofibromatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile Nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile Nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Self-limited familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early Infantile Epileptic Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early Infantile Epileptic Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal Infantile Cardioencephalomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal Infantile Cardioencephalomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Periodic fever-infantile enterocolitis-autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever-infantile enterocolitis-autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile osteopetrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile osteopetrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic Infantile Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic Infantile Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IL21-related infantile inflammatory bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IL21-related infantile inflammatory bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epileptic dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epileptic dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile or childhood onset neurodegenerative disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset generalized dyskinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset generalized dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient infantile hypertriglyceridemia and hepatosteatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient infantile hypertriglyceridemia and hepatosteatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic kinesigenic dyskinesia and familial infantile convulsions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia and familial infantile convulsions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Idiopathic Infantile Hypercalcemia - Mild Form Gene Set

Idiopathic hypercalcemia of infancy Gene Set

infantile hypercalcemia Gene Set

hypercalcemia, infantile Gene Set

Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set

Infantile hypercalcemia Gene Set

Autosomal recessive infantile hypercalcemia Gene Set

Idiopathic fibrosing alveolitis, chronic form Gene Set

juvenile polyposis syndrome, infantile form Gene Set

Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set

Hypercalciuric hypercalcemia Gene Set

Familial benign hypercalcemia Gene Set

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

Hypocalciuric hypercalcemia, familial, type 2 Gene Set

Hypocalciuric hypercalcemia, familial, type 3 Gene Set

Hypercalcemia Gene Set

Familial benign hypercalcemia, type 3 Gene Set

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

hypercalcemia Gene Set

chronic renal failure; hypercalcemia; kidney failure, chronic Gene Set

hypercalcemia; hyperparathyroidism, primary Gene Set

hypercalcemia; hypercalciuria Gene Set

hypercalcemia; sarcoidosis, pulmonary Gene Set

familial hypocalciuric hypercalcemia Gene Set

hypercalcemia Gene Set

hypercalcemia Gene Set

Hypercalcemia Gene Set

hypercalciuric hypercalcemia Gene Set

hypocalciuric hypercalcemia, type i Gene Set

hypocalciuric hypercalcemia, type ii Gene Set

hypocalciuric hypercalcemia, familial, type iii Gene Set

humoral hypercalcemia of malignancy Gene Set

Hypercalcemia Gene Set

Familial Benign Hypercalcemia Gene Set

Humoral Hypercalcemia Of Malignancy (Disorder) Gene Set

Hypocalciuric Hypercalcemia Gene Set

Hypocalciuric Hypercalcemia, Acquired Gene Set

Hypercalcemia Gene Set

Hypercalcemia Gene Set

Familial hypocalciuric hypercalcemia Gene Set

Familial hypocalciuric hypercalcemia 1 Gene Set

Familial hypocalciuric hypercalcemia 2 Gene Set

Familial hypocalciuric hypercalcemia 3 Gene Set

Familial hypocalciuric hypercalcemia Gene Set

Hypercalcemia Gene Set

Congenital myotonia, autosomal dominant form Gene Set

Osteogenesis imperfecta with normal sclerae, dominant form Gene Set

Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set

NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set

Congenital myotonia, autosomal recessive form Gene Set

NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set

GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set

Vohwinkel Syndrome, Variant Form Gene Set

Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set

Hepatorenal form of glycogen storage disease Gene Set

Ehlers-Danlos syndrome, cardiac valvular form Gene Set

Ehlers-Danlos syndrome, progeroid form Gene Set

form agnosia Gene Set

1,6-Fructose Diphosphate (Linear Form) Gene Set

immunologically hyper-reactive form of onchocerciasis (sowda) Gene Set

hyper-igm syndrome can form oligomers and trigger cd40-mediated signals Gene Set

form Gene Set

y-form dna binding Gene Set

latanoprost (free acid form) Gene Set

misoprostol (free acid form) Gene Set

butaprost (free acid form) Gene Set

bimatoprost (free acid form) Gene Set

abnormal form of the vertebral bodies Gene Set

PLUNC, long form Gene Set

Phenylalanine-4-hydroxylase, tetrameric form Gene Set

failure to form blastocele Gene Set

failure to form egg cylinders Gene Set

ehlers-danlos syndrome, cardiac valvular form Gene Set

polyglucosan body disease, adult form Gene Set

organism form Gene Set

plant form Gene Set

organism form Gene Set

plant form Gene Set

procyclic form Gene Set