Episodic Generalized Hypotonia

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Results for "Episodic Generalized Hypotonia": 487 gene sets

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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 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 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 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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia, type 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Choreoathetosis/spasticity, episodic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Choreoathetosis/spasticity, episodic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic ataxia type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic Kinesigenic Dyskinesia 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Kinesigenic Dyskinesia 1 from the curated CTD Gene-Disease Associations dataset.
Episodic ataxia with nystagmus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic ataxia with nystagmus from the curated CTD Gene-Disease Associations dataset.
Episodic Muscle Weakness, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis/Spasticity, Episodic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis/Spasticity, Episodic from the curated CTD Gene-Disease Associations dataset.
Congenital myasthenic syndrome with episodic apnea Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 3 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 1 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 7 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 5 from the curated CTD Gene-Disease Associations dataset.
Episodic Ataxia, Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 6 from the curated CTD Gene-Disease Associations dataset.
Episodic Kinesigenic Dyskinesia 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Kinesigenic Dyskinesia 2 from the curated CTD Gene-Disease Associations dataset.
episodic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease episodic ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
episodic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
episodic ataxia type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease episodic ataxia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
episodic memory Gene Set From GAD Gene-Disease Associations genes associated with the disease episodic memory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
episodic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term episodic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
episodic tachypnea Gene Set From HPO Gene-Disease Associations genes associated with the episodic tachypnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ataxia Gene Set From HPO Gene-Disease Associations genes associated with the episodic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic flaccid weakness Gene Set From HPO Gene-Disease Associations genes associated with the episodic flaccid weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ketoacidosis Gene Set From HPO Gene-Disease Associations genes associated with the episodic ketoacidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic hyperhidrosis Gene Set From HPO Gene-Disease Associations genes associated with the episodic hyperhidrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sudden episodic apnea Gene Set From HPO Gene-Disease Associations genes associated with the sudden episodic apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic vomiting Gene Set From HPO Gene-Disease Associations genes associated with the episodic vomiting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic hypertension Gene Set From HPO Gene-Disease Associations genes associated with the episodic hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic upper airway obstruction Gene Set From HPO Gene-Disease Associations genes associated with the episodic upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the episodic peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intrahepatic cholestasis with episodic jaundice Gene Set From HPO Gene-Disease Associations genes associated with the intrahepatic cholestasis with episodic jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic fever Gene Set From HPO Gene-Disease Associations genes associated with the episodic fever phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the episodic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic metabolic acidosis Gene Set From HPO Gene-Disease Associations genes associated with the episodic metabolic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic abdominal pain Gene Set From HPO Gene-Disease Associations genes associated with the episodic abdominal pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic hemiplegia Gene Set From HPO Gene-Disease Associations genes associated with the episodic hemiplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ammonia intoxication Gene Set From HPO Gene-Disease Associations genes associated with the episodic ammonia intoxication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic hemolytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the episodic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic ataxia, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic kinesigenic dyskinesia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic kinesigenic dyskinesia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic kinesigenic dyskinesia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic kinesigenic dyskinesia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic muscle weakness, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic ataxia/myokymia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the episodic ataxia/myokymia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, congenital, associated with episodic apnea Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset.
Episodic Kinesigenic Dyskinesia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Kinesigenic Dyskinesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Episodic Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Episodic Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Quadriplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrahepatic Cholestasis With Episodic Jaundice Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholestasis With Episodic Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Cluster Headache Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Cluster Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Tension-Type Headache Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Tension-Type Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Paroxysmal Anxiety Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Paroxysmal Anxiety in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Pain Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Pain Syndrome 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.
Choreoathetosis/Spasticity, Episodic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choreoathetosis/Spasticity, Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Hemolytic Anemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Vomiting Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Vomiting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Metabolic Acidosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Metabolic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Tachypnea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Tachypnea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Ketoacidosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ketoacidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Respiratory Distress Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Respiratory Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Hyperhidrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hyperhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Ammonia Intoxication Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ammonia Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Hemiplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hemiplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Abdominal Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Flaccid Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Flaccid Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Hypokalemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypokalemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Memory, Episodic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory, Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Upper Airway Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Hypertension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Hypoventilation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC1A3 causes episodic ataxia 6 (EA6) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC1A3 causes episodic ataxia 6 (EA6) pathway from the Reactome Pathways 2024 dataset.
Episodic ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Episodic kinesigenic dyskinesia 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic kinesigenic dyskinesia 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Episodic kinesigenic dyskinesia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic kinesigenic dyskinesia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic kinesigenic dyskinesia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic kinesigenic dyskinesia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic ataxia type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Episodic hemiplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic hemiplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary episodic ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic kinesigenic dyskinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial episodic pain syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial episodic pain syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic pain syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic pain syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic flaccid weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic flaccid weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic vomiting Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic vomiting phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic kinesigenic dyskinesia and familial infantile convulsions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia and familial infantile convulsions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic memory Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Episodic memory phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Language performance in older adults (adjusted for episodic memory) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Language performance in older adults (adjusted for episodic memory) 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

Episodic Generalized Hypotonia Gene Set

generalized hypotonia Gene Set

generalized hypotonia Gene Set

generalized neonatal hypotonia Gene Set

generalized hypotonia due to defect at the neuromuscular junction Gene Set

Generalized Hypotonia Gene Set

Generalized Neonatal Hypotonia Gene Set

Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set

Generalized hypotonia 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

neonatal 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

Neonatal Hypotonia 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

History of neonatal hypotonia Gene Set

Spastic tetraplegia and axial hypotonia Gene Set

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

Neonatal hypotonia 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

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

Congenital hypotonia Gene Set

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

Unilateral Hypotonia Gene Set

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set

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

Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set