Refractory Infantile Spasms

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Results for "Refractory Infantile Spasms": 436 gene sets

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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.
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.
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.
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 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.
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.
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.
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 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.
anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
spasms Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spasms in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
myoclonic spasms Gene Set From GWASdb SNP-Phenotype Associations genes associated with the myoclonic spasms phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
epileptic spasms Gene Set From HPO Gene-Disease Associations genes associated with the epileptic spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myoclonic spasms Gene Set From HPO Gene-Disease Associations genes associated with the myoclonic spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Late-Onset Epileptic Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Late-Onset Epileptic Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Spasms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myoclonic Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Painful Muscle Spasms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Painful Muscle Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Spasms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autosomal recessive hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Iron-Refractory Iron Deficiency Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.
Anemia, Refractory Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Refractory from the curated CTD Gene-Disease Associations dataset.
refractory hairy cell leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease refractory hairy cell leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
refractory hematologic cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease refractory hematologic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
refractory Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term refractory in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Schizophrenia (treatment refractory) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia (treatment refractory) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
refractory anemia Gene Set From HPO Gene-Disease Associations genes associated with the refractory anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
refractory macrocytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the refractory macrocytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Anemia, Refractory, with Excess of Blasts Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Anemia, Refractory, with Excess of Blasts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Anemia, Refractory Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Anemia, Refractory phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
?anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ?anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
iron-refractory iron deficiency anemia Gene Set From OMIM Gene-Disease Associations genes associated with the iron-refractory iron deficiency anemia phenotype from the curated OMIM Gene-Disease Associations dataset.
Refractory Cytopenia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hormone Refractory Prostate Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hormone Refractory Prostate Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Anemias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Anemias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Colorectal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Anemia With Excess Blasts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Anemia With Excess Blasts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iron-Refractory Iron Deficiency Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iron-Refractory Iron Deficiency Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Acute Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Acute Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Breast Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Lung Non-Small Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Lung Non-Small Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Celiac Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Large B-Cell Lymphoma Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Adult Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Adult Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Follicular Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cytopenia With Multilineage Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia With Multilineage Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Osteosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Lymphocytic Leukaemia Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Lymphocytic Leukaemia Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hormone Refractory Breast Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hormone Refractory Breast Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mantle Cell Lymphoma Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mantle Cell Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Erdheim-Chester Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Erdheim-Chester Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Hairy Cell Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Hairy Cell Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Thyroid Gland Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marginal Zone Lymphoma Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marginal Zone Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult T-Cell Lymphoma/Leukaemia Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult T-Cell Lymphoma/Leukaemia Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Angioimmunoblastic T-Cell Lymphoma Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Angioimmunoblastic T-Cell Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cytopenia With Multilineage Dysplasia (Rcmd) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia With Multilineage Dysplasia (Rcmd) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Hodgkin'S Lymphoma Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory B Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Head And Neck Squamous Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Head And Neck Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Kaposi Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Kaposi Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Nasopharyngeal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Nasopharyngeal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Severe Refractory Exacerbation Of Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Severe Refractory Exacerbation Of Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Neuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Synovial Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Synovial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Ewing Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Ewing Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Mature T-Cell And Nk-Cell Non-Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Mature T-Cell And Nk-Cell Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Steroid Refractory Graft Versus Host Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Steroid Refractory Graft Versus Host Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures In The Newborn, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Seizures In The Newborn, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Angina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Angina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Grand Mal Status Epilepticus, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Grand Mal Status Epilepticus, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Waldenstrom'S Macroglobulinaemia Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Waldenstrom'S Macroglobulinaemia Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Frontal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Frontal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Occipital Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Occipital Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Macrocytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Macrocytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Juvenile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Juvenile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cytopenia With Multilineage Dysplasia And Ringed Sideroblasts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia With Multilineage Dysplasia And Ringed Sideroblasts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Heart Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Bladder Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Bladder Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Urothelial Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Urothelial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cancer Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Refractory Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
New-Onset Refractory Status Epilepticus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype New-Onset Refractory Status Epilepticus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Refractory Chronic Cough Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Refractory Chronic Cough in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Refractory Angina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Refractory Angina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Refractory plasma cell neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Refractory plasma cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
relapsed/refractory diffuse large B-cell lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease relapsed/refractory diffuse large B-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Refractory hematologic cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Refractory hematologic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Refractory hairy cell leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Refractory hairy cell leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Refractory T lymphoblastic leukemia/lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Refractory T lymphoblastic leukemia/lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Iron-refractory iron deficiency anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron-refractory iron deficiency anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Refractory anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Refractory anemia phenotype from the curated ClinVar Gene-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.
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.
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.
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 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.
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 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.
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.
hypercalcemia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypercalcemia, infantile 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.
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.
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.
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 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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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

Refractory Infantile Spasms Gene Set

Spasms, Infantile Gene Set

neurofibromatosis 1; spasms, infantile Gene Set

spasms, infantile Gene Set

infantile spasms Gene Set

Spasms, Infantile Gene Set

Cryptogenic Infantile Spasms Gene Set

Symptomatic Infantile Spasms Gene Set

Infantile spasms Gene Set

anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set

Early Infantile Epileptic Encephalopathy, Refractory Gene Set

Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set

spasms Gene Set

myoclonic spasms Gene Set

epileptic spasms Gene Set

myoclonic spasms Gene Set

Spasms Gene Set

Cryptogenic Late-Onset Epileptic Spasms Gene Set

Myoclonic Spasms Gene Set

Intermittent Painful Muscle Spasms Gene Set

Generalized Spasms Gene Set

Autosomal recessive hypophosphatemic vitamin D refractory rickets Gene Set

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Gene Set

Iron-Refractory Iron Deficiency Anemia Gene Set

Anemia, Refractory Gene Set

refractory hairy cell leukemia Gene Set

refractory hematologic cancer Gene Set

anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set

refractory Gene Set

Schizophrenia (treatment refractory) Gene Set

refractory anemia Gene Set

refractory macrocytic anemia Gene Set

Anemia, Refractory, with Excess of Blasts Gene Set

Anemia, Refractory Gene Set

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

?anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

iron-refractory iron deficiency anemia Gene Set

Refractory Cytopenia Of Childhood Gene Set

Hormone Refractory Prostate Cancer Gene Set

Refractory Anemias Gene Set

Refractory Colorectal Carcinoma Gene Set

Refractory Lymphoma Gene Set

Refractory Anemia With Excess Blasts Gene Set

Refractory Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene Set

Refractory Acute Lymphoblastic Leukemia Gene Set

Refractory Thrombocytopenia Gene Set

Iron-Refractory Iron Deficiency Anemia Gene Set

Refractory Acute Leukemia Gene Set

Refractory Sarcoma Gene Set

Refractory Breast Carcinoma Gene Set

Refractory Lung Non-Small Cell Carcinoma Gene Set

Refractory Celiac Disease Gene Set

Diffuse Large B-Cell Lymphoma Refractory Gene Set

Refractory Adult Acute Lymphoblastic Leukemia Gene Set

Refractory Childhood Acute Lymphoblastic Leukemia Gene Set

Refractory Childhood Hodgkin Lymphoma Gene Set

Refractory Follicular Lymphoma Gene Set

Refractory Hodgkin Lymphoma Gene Set

Refractory Leukemia Gene Set

Refractory Cytopenia With Multilineage Dysplasia Gene Set

Refractory Osteosarcoma Gene Set

Chronic Lymphocytic Leukaemia Refractory Gene Set

Hormone Refractory Breast Cancer Gene Set

Mantle Cell Lymphoma Refractory Gene Set

Refractory Neoplasm Gene Set

Refractory Erdheim-Chester Disease Gene Set

Refractory Hairy Cell Leukemia Gene Set

Refractory Melanoma Gene Set

Refractory Thyroid Gland Carcinoma Gene Set

Marginal Zone Lymphoma Refractory Gene Set

Refractory Classic Hodgkin Lymphoma Gene Set

Adult T-Cell Lymphoma/Leukaemia Refractory Gene Set

Angioimmunoblastic T-Cell Lymphoma Refractory Gene Set

Refractory Cytopenia With Multilineage Dysplasia (Rcmd) Gene Set

Non-Hodgkin'S Lymphoma Refractory Gene Set

Refractory B Acute Lymphoblastic Leukemia Gene Set