Generalized neonatal hypotonia

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Results for "Generalized neonatal hypotonia": 652 gene sets

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generalized neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Generalized Neonatal Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
History of neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the History of neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
generalized hypotonia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypotonia due to defect at the neuromuscular junction Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Episodic Generalized Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Generalized Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscle Hypotonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscle Hypotonia from the curated CTD Gene-Disease Associations dataset.
Hypotonia-Cystinuria Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotonia-Cystinuria Syndrome from the curated CTD Gene-Disease Associations dataset.
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypotonia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hypotonia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
muscular hypotonia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the muscular hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
central hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the central hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
facial hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the facial hypotonia 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.
muscular hypotonia of the trunk Gene Set From HPO Gene-Disease Associations genes associated with the muscular hypotonia of the trunk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the severe muscular hypotonia 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.
Muscle Hypotonia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscle Hypotonia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hypotonia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hypotonia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hypotonia-cystinuria syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hypotonia-cystinuria syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Atypical Hypotonia Cystinuria Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Hypotonia Cystinuria Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unilateral Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unilateral Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Hypotonia Of The Trunk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Hypotonia Of The Trunk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype 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.
Appendicular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Appendicular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Oral Motor Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oral Motor Hypotonia 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.
hypotonia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hypotonia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hypotonia-cystinuria syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotonia-cystinuria syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hypotonia, ataxia, and delayed development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotonia, ataxia, and delayed development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital limbs-face contractures-hypotonia-developmental delay syndrome 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.
Developmental delay, hypotonia, and impaired language Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay, hypotonia, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic tetraplegia and axial hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia and axial hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-hypotonia-spasticity-sleep disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiomyopathy-hypotonia-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiomyopathy-hypotonia-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-hypotonia-movement disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-hypotonia-movement disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Unilateral Hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Unilateral Hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome 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.
Axial hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Axial hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe muscular hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe muscular hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient neonatal diabetes mellitus 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Transient neonatal diabetes mellitus 1 phenotype from the curated ClinVar Gene-Phenotype Associations 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.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperparathyroidism, neonatal severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperparathyroidism, neonatal severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with neurologic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal adrenoleucodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal adrenoleucodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cyanosis, transient neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cyanosis, transient neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset.
Hyperparathyroidism, Neonatal Severe Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset.
Neonatal-onset citrullinemia type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Jaundice, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Neonatal from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 1 from the curated CTD Gene-Disease Associations dataset.
Finnish lethal neonatal metabolic syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 2 from the curated CTD Gene-Disease Associations dataset.
Pancreatic beta cell agenesis with neonatal diabetes mellitus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pancreatic beta cell agenesis with neonatal diabetes mellitus from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal from the curated CTD Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal Abstinence Syndrome from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Anemia, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Neonatal from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Neonatal Alloimmune from the curated CTD Gene-Disease Associations dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal period electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal thrombocytopenia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal; jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal; jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cutaneous neonatal lupus Gene Set From GAD Gene-Disease Associations genes associated with the disease cutaneous neonatal lupus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute neonatal disease and hyperammonemia Gene Set From GAD Gene-Disease Associations genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neonatal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
neonatal unconjugated hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal unconjugated hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal breathing dysregulation Gene Set From HPO Gene-Disease Associations genes associated with the neonatal breathing dysregulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal alloimmune thrombocytopenia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal alloimmune thrombocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal epiphyseal stippling Gene Set From HPO Gene-Disease Associations genes associated with the neonatal epiphyseal stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal death Gene Set From HPO Gene-Disease Associations genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal insulin-dependent diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the neonatal insulin-dependent diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal wrinkled skin of hands and feet Gene Set From HPO Gene-Disease Associations genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spontaneous neonatal pneumothorax Gene Set From HPO Gene-Disease Associations genes associated with the spontaneous neonatal pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal respiratory distress Gene Set From HPO Gene-Disease Associations genes associated with the neonatal respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
transient neonatal diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the transient neonatal diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal short-limb short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prolonged neonatal jaundice Gene Set From HPO Gene-Disease Associations genes associated with the prolonged neonatal jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hypoglycemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal onset Gene Set From HPO Gene-Disease Associations genes associated with the neonatal onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neonatal Abstinence Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Jaundice, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Jaundice, Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Benign Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Benign Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hyperbilirubinemia, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperbilirubinemia, Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thrombocytopenia, Neonatal Alloimmune phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
partial neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
diabetes mellitus, neonatal, with congenital hypothyroidism Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, neonatal, with congenital hypothyroidism phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
?diabetes mellitus, insulin-dependent, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the ?diabetes mellitus, insulin-dependent, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, neonatal hemolytic, fatal and near-fatal Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, neonatal hemolytic, fatal and near-fatal phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia gravis, neonatal transient Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia gravis, neonatal transient phenotype from the curated OMIM Gene-Disease Associations dataset.
cpt ii deficiency, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cpt ii deficiency, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{diabetes mellitus, transient neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {diabetes mellitus, transient neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, neonatal severe Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune, bak antigen related Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune, bak antigen related phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
citrullinemia, type ii, neonatal-onset Gene Set From OMIM Gene-Disease Associations genes associated with the citrullinemia, type ii, neonatal-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal, with neurologic features Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated OMIM Gene-Disease Associations dataset.
choreoathetosis, hypothyroidism, and neonatal respiratory distress Gene Set From OMIM Gene-Disease Associations genes associated with the choreoathetosis, hypothyroidism, and neonatal respiratory distress phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypertrypsinemia, neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypertrypsinemia, neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, alloimmune neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, alloimmune neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary hypertension, neonatal, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, neonatal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
zinc deficiency, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the zinc deficiency, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
cyanosis, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cyanosis, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
neonatal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term neonatal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Neonatal Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Abstinence Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hepatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
K Atp Permanent Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease K Atp Permanent Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenoleukodystrophy, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adrenoleukodystrophy, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Cholangitis, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Cholangitis, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Herpes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Herpes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Opiate Withdrawal Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Opiate Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Inflammatory Skin And Bowel Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Inflammatory Skin And Bowel Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Citrullinemia, Type Ii, Neonatal-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Citrullinemia, Type Ii, Neonatal-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemochromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Systemic Lupus Erythematosus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Systemic Lupus Erythematosus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Renal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Chlamydial Conjunctivitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Chlamydial Conjunctivitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Early-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Early-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alloimmune Neonatal Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alloimmune Neonatal Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombocytopenia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombocytopenia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Onset Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Onset Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Late-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Late-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Torulopsis Glabrata Fungemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Torulopsis Glabrata Fungemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Marfan Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Marfan Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noninfective Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noninfective Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Necrotizing Enterocolitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Necrotizing Enterocolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Respiratory System Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory System Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Leukaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Leukaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cyanosis, Transient Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cyanosis, Transient Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indirect Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indirect Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia (Nait) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia (Nait) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Maladjustment Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Maladjustment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy, Nonfamilial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy, Nonfamilial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Listeriosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Listeriosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombosis Of Cerebral Venous Sinus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombosis Of Cerebral Venous Sinus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Unconjugated Hyperbilirubinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Unconjugated Hyperbilirubinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
6Q24-Related Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 6Q24-Related Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Testicular Torsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Testicular Torsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngospasm, Severe Neonatal Episodic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngospasm, Severe Neonatal Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Disorder Of Endocrine System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Disorder Of Endocrine System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperthyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperthyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thyrotoxicosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thyrotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prolonged Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Respiratory Distress Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Respiratory Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Insulin-Dependent Diabetes Mellitus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Insulin-Dependent Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tremor, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tremor, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spontaneous Neonatal Pneumothorax Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Neonatal Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Breathing Dysregulation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Breathing Dysregulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Cholestatic Liver Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Cholestatic Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Wrinkled Skin Of Hands And Feet Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Wrinkled Skin Of Hands And Feet in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypertrypsinemia, Neonatal, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypertrypsinemia, Neonatal, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Short-Limb Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Short-Trunk Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Direct Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Direct Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Epiphyseal Stippling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Epiphyseal Stippling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neonatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Neonatal astrocyte_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neonatal astrocyte_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Benign neonatal seizures Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neonatal seizures from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal diabetes from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Permanent neonatal diabetes mellitus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Permanent neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal period electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
neonatal-onset type II citrullinemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease neonatal-onset type II citrullinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal diabetes mellitus with congenital hypothyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes mellitus with congenital hypothyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal infective mastitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal infective mastitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal intrahepatic cholestasis due to citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency 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.
Neonatal severe primary hyperparathyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal severe primary hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transitory neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transitory neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient Neonatal Diabetes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient Neonatal Diabetes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal Marfan syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal Marfan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign neonatal seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign neonatal seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Neonatal Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Neonatal Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal pseudo-hydrocephalic progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal pseudo-hydrocephalic progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypoglycemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypoglycemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated neonatal sclerosing cholangitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated neonatal sclerosing cholangitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal ichthyosis-sclerosing cholangitis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal and neonatal alloimmune thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal and neonatal alloimmune thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal respiratory distress Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal respiratory distress phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal inflammatory skin and bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal inflammatory skin and bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal white matter microstructure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal white matter microstructure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyrotropin-releasing hormone resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyrotropin-releasing hormone resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized arterial calcification of infancy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized arterial calcification of infancy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pustular psoriasis, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pustular psoriasis, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Generalized from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 6 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 1 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 3 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 4 from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis congenital generalized X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 2 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.
generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease generalized dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glucose tolerance; lipids; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose tolerance; lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, generalized; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, generalized; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intima-media thickness; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease intima-media thickness; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; epilepsy, generalized; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 2; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, reflex Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, reflex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease generalized epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, tonic-clonic Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized epimerase-deficiency galactosemia Gene Set From GAD Gene-Disease Associations genes associated with the disease generalized epimerase-deficiency galactosemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsies, partial; epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsies, partial; epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipids; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term generalized in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Generalized seizures_Brain_GSE6614 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Generalized seizures_Brain_GSE6614 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Epilepsy (generalized) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Epilepsy (generalized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
generalized amyloid deposition Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized amyloid deposition phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
moderate generalized osteoporosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the moderate generalized osteoporosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized abnormality of skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized osteosclerosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized osteosclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
eeg with generalized epileptiform discharges Gene Set From HPO Gene-Disease Associations genes associated with the eeg with generalized epileptiform discharges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized osteosclerosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized limb muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperreflexia Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperreflexia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized abnormality of skin Gene Set From HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized bone demineralization Gene Set From HPO Gene-Disease Associations genes associated with the generalized bone demineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized morning stiffness Gene Set From HPO Gene-Disease Associations genes associated with the generalized morning stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscle hypertrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscle hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized arterial tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the generalized arterial tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized opacification of the cornea Gene Set From HPO Gene-Disease Associations genes associated with the generalized opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hirsutism Gene Set From HPO Gene-Disease Associations genes associated with the generalized hirsutism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypopigmentation of hair Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized aminoaciduria Gene Set From HPO Gene-Disease Associations genes associated with the generalized aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized seborrheic dermatitis Gene Set From HPO Gene-Disease Associations genes associated with the generalized seborrheic dermatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized myoclonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized myoclonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized dystonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized arterial calcification Gene Set From HPO Gene-Disease Associations genes associated with the generalized arterial calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized edema Gene Set From HPO Gene-Disease Associations genes associated with the generalized edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with generalized slow activity Gene Set From HPO Gene-Disease Associations genes associated with the eeg with generalized slow activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intermittent generalized erythematous papular rash Gene Set From HPO Gene-Disease Associations genes associated with the intermittent generalized erythematous papular rash phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic-clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic-clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperkeratosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized osteoporosis with pathologic fractures Gene Set From HPO Gene-Disease Associations genes associated with the generalized osteoporosis with pathologic fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypopigmentation Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypopigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized papillary lesions Gene Set From HPO Gene-Disease Associations genes associated with the generalized papillary lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized distal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscular appearance from birth Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized joint laxity Gene Set From HPO Gene-Disease Associations genes associated with the generalized joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital, generalized hypertrichosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital, generalized hypertrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized lipodystrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized lipodystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized amyloid deposition Gene Set From HPO Gene-Disease Associations genes associated with the generalized amyloid deposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Epilepsy, Generalized Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Generalized phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy and paroxysmal dyskinesia Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilespy, generalized, with febrile seizures plus, type 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epilespy, generalized, with febrile seizures plus, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy with febrile seizures plus, type 9 Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
thyrotropin-releasing hormone resistance, generalized Gene Set From OMIM Gene-Disease Associations genes associated with the thyrotropin-releasing hormone resistance, generalized phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?lipodystrophy, congenital generalized, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, congenital generalized, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epidermolysis bullosa, generalized atrophic benign Gene Set From OMIM Gene-Disease Associations genes associated with the epidermolysis bullosa, generalized atrophic benign phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis, congenital generalized Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis, congenital generalized phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
arterial calcification, generalized, of infancy, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arterial calcification, generalized, of infancy, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arterial calcification, generalized, of infancy, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arterial calcification, generalized, of infancy, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Generalized Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Myoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Enlarged Lymph Nodes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Enlarged Lymph Nodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Anxiety Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Anxiety Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hypopigmentation Of Hair Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Hypopigmentation Of Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aggressive Periodontitis, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Periodontitis, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Glycogen Storage Disease Of Infants Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Glycogen Storage Disease Of Infants in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Vitiligo Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Vitiligo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Limb Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Chronic Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Chronic Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Thyroid Hormone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Thyroid Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Pustular Psoriasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Pustular Psoriasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anxiety Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anxiety Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Tetanus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tetanus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Morphea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Morphea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Seborrheic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Seborrheic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Convulsive Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Convulsive Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Nonconvulsive Seizure Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Nonconvulsive Seizure Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Generalized Exanthematous Pustulosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Generalized Exanthematous Pustulosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Obesity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia Gravis, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia Gravis, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Myotonia Of Thomsen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Myotonia Of Thomsen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Generalized Myotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Generalized Myotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Abnormality Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Abnormality Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Dystrophic Epidermolysis Bullosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Dystrophic Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Generalized Recessive Dystrophic Epidermolysis Bullosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Generalized Recessive Dystrophic Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Tonic-Clonic Seizures With Focal Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tonic-Clonic Seizures With Focal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytosis, Generalized Eruptive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytosis, Generalized Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Distal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy And Paroxysmal Dyskinesia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy And Paroxysmal Dyskinesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, 7 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus, 7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Social Phobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Social Phobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hypotrichosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyrotropin-Releasing Hormone Resistance, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyrotropin-Releasing Hormone Resistance, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Weakness, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hirsutism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hirsutism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Epileptiform Discharges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Epileptiform Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Weakness Of Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Weakness Of Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Irregular Generalized Spike And Wave Complexes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Irregular Generalized Spike And Wave Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscular Appearance From Birth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscular Appearance From Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hyperkeratosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperkeratosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Bone Demineralization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Bone Demineralization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Amyloid Deposition Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Amyloid Deposition in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypertrichosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypertrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Pruritus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Pruritus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Morning Stiffness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Morning Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic-Clonic Seizures On Awakening Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic-Clonic Seizures On Awakening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Slow Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Slow Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Osteosclerosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Osteosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Generalized Osteoporosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Generalized Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Headache Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Aminoaciduria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Aminoaciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Bronze Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Bronze Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Wasting Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Wasting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hyperreflexia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperreflexia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Arterial Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Arterial Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Polyspikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Polyspikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Arterial Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Arterial Calcification 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.
Generalized Hypopigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Papillary Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Papillary Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Anhidrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Anhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Microdontia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Microdontia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Generalized Erythematous Papular Rash Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Generalized Erythematous Papular Rash in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Reticulate Brown Pigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Reticulate Brown Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
generalized edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the generalized edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Congenital generalized lipodystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Congenital generalized lipodystrophy pathway from the WikiPathways Pathways 2024 dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complete generalized lipodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized epilepsy with febrile seizures plus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent generalized lymphadenopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent generalized lymphadenopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complete generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized lymphatic anomaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epidermolysis bullosa simplex generalized type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epidermolysis bullosa simplex generalized type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bilateral generalized polymicrogyria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral generalized polymicrogyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital generalized lipodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital generalized lipodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset generalized limb-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset generalized limb-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized juvenile polyposis/juvenile polyposis coli Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized juvenile polyposis/juvenile polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized pustular psoriasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized pustular psoriasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy-paroxysmal dyskinesia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy-paroxysmal dyskinesia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized-onset seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized-onset seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hypopigmentation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypopigmentation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized myoclonic seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized myoclonic seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN2A-related generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN2A-related generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hyperreflexia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hyperreflexia 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.
Generalized hypertrichosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypertrichosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized choriocapillaris dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized choriocapillaris dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Response to antiepileptic drugs in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antiepileptic drugs in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to levetiracetam in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to levetiracetam in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine and valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine and valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

generalized neonatal hypotonia Gene Set

Generalized Neonatal Hypotonia Gene Set

neonatal hypotonia Gene Set

Neonatal Hypotonia Gene Set

History of neonatal hypotonia Gene Set

Neonatal hypotonia Gene Set

PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene Set

PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set

generalized hypotonia Gene Set

generalized hypotonia Gene Set

generalized hypotonia due to defect at the neuromuscular junction Gene Set

Episodic Generalized Hypotonia Gene Set

Generalized Hypotonia Gene Set

Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set

Generalized hypotonia Gene Set

encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set

jaundice, neonatal; neonatal jaundice Gene Set

glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

Muscle Hypotonia Gene Set

Hypotonia-Cystinuria Syndrome Gene Set

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

hypotonia Gene Set

muscular hypotonia Gene Set

central hypotonia Gene Set

muscular hypotonia Gene Set

facial hypotonia Gene Set

infantile muscular hypotonia Gene Set

muscular hypotonia of the trunk Gene Set

severe muscular hypotonia Gene Set

infantile axial hypotonia Gene Set

Muscle Hypotonia Gene Set

hypotonia Gene Set

hypotonia-cystinuria syndrome Gene Set

?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

Atypical Hypotonia Cystinuria Syndrome Gene Set

Hypotonia Gene Set

Benign Congenital Hypotonia Gene Set

Hydronephrosis, Congenital, With Cleft Palate, Characteristic Facies, Hypotonia, And Mental Retardation Gene Set

Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set

Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set

Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set

Muscle Hypotonia Gene Set

Severe Muscular Hypotonia Gene Set

Unilateral Hypotonia Gene Set

Muscular Hypotonia Of The Trunk Gene Set

Infantile Muscular Hypotonia Gene Set

Appendicular Hypotonia Gene Set

Hypotonia Gene Set

Central Hypotonia Gene Set

Facial Hypotonia Gene Set

Oral Motor Hypotonia Gene Set

Infantile Axial Hypotonia Gene Set

hypotonia Gene Set

hypotonia-cystinuria syndrome Gene Set

hypotonia, ataxia, and delayed development syndrome Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set

Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set

Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set

Infantile hypotonia with psychomotor retardation and characteristic facies-3 Gene Set

Developmental delay, hypotonia, and impaired language Gene Set

Central hypotonia Gene Set

Hypotonia Gene Set

Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set

Spastic tetraplegia and axial hypotonia Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

Intellectual disability-hypotonia-spasticity-sleep disorder syndrome Gene Set

Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set

Cardiomyopathy-hypotonia-lactic acidosis syndrome Gene Set

Congenital hypotonia Gene Set

X-linked intellectual disability-hypotonia-movement disorder syndrome Gene Set