atrioventricular block; myotonic dystrophy

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Results for "atrioventricular block; myotonic dystrophy": 1001 gene sets

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atrioventricular block; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrioventricular block; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Electrocardiogram Atrioventricular Block Complete Heart Block Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electrocardiogram Atrioventricular Block Complete Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrioventricular Block Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Block from the curated CTD Gene-Disease Associations dataset.
atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set From GAD Gene-Disease Associations genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
third degree atrioventricular block Gene Set From HPO Gene-Disease Associations genes associated with the third degree atrioventricular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
first degree atrioventricular block Gene Set From HPO Gene-Disease Associations genes associated with the first degree atrioventricular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular block Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Atrioventricular Block Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Atrioventricular Block phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
atrioventricular block Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrioventricular block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Complete Atrioventricular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Atrioventricular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
First Degree Atrioventricular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease First Degree Atrioventricular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Second Degree Atrioventricular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Second Degree Atrioventricular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
atrioventricular block Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular block phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
second-degree atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease second-degree atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
third-degree atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease third-degree atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
first-degree atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease first-degree atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mobitz type II atrioventricular block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mobitz type II atrioventricular block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrioventricular block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Third degree atrioventricular block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Third degree atrioventricular block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
First degree atrioventricular block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the First degree atrioventricular block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular septal defect and common atrioventricular junction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myotonic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myotonic Dystrophy from the curated CTD Gene-Disease Associations dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromyalgia; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromyalgia; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Myotonic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myotonic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic dystrophy protein kinase, coiled coil Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myotonic dystrophy protein kinase, coiled coil protein domain from the InterPro Predicted Protein Domain Annotations dataset.
myotonic dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy type1 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myotonic dystrophy type1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myotonic dystrophy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myotonic dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myotonic dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Steinert myotonic dystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Steinert myotonic dystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myotonic dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myotonic dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
myotonic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myotonic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myotonic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term myotonic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
emg: myotonic runs Gene Set From HPO Gene-Disease Associations genes associated with the emg: myotonic runs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Myotonic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myotonic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Emg: Myotonic Runs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Emg: Myotonic Runs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Emg: Myotonic Discharges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Emg: Myotonic Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Myotonic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myotonic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myotonic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myotonic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
becker muscular dystrophy; duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart block, nonprogressive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Heart block, nonprogressive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
pluronic block copolymer p85 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical pluronic block copolymer p85 from the curated CTD Gene-Chemical Interactions dataset.
Heart Block Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heart Block from the curated CTD Gene-Disease Associations dataset.
Sinoatrial Block Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sinoatrial Block from the curated CTD Gene-Disease Associations dataset.
Bundle-Branch Block Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bundle-Branch Block from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
congenital heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
right bundle branch block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease right bundle branch block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive av-block and anomalous venous return Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive av-block and anomalous venous return in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune-associated congenital heart block. Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune-associated congenital heart block. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
block Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term block in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
heart block Gene Set From GWASdb SNP-Phenotype Associations genes associated with the heart block phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
left bundle branch block Gene Set From HPO Gene-Disease Associations genes associated with the left bundle branch block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
left anterior fascicular block Gene Set From HPO Gene-Disease Associations genes associated with the left anterior fascicular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete heart block with broad rs complexes Gene Set From HPO Gene-Disease Associations genes associated with the complete heart block with broad rs complexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
heart block Gene Set From HPO Gene-Disease Associations genes associated with the heart block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
block vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the block vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bundle branch block Gene Set From HPO Gene-Disease Associations genes associated with the bundle branch block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right bundle branch block Gene Set From HPO Gene-Disease Associations genes associated with the right bundle branch block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
left postterior fascicular block Gene Set From HPO Gene-Disease Associations genes associated with the left postterior fascicular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Heart Block Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Heart Block phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bundle-Branch Block Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bundle-Branch Block phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
B-block binding subunit of TFIIIC Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the B-block binding subunit of TFIIIC protein domain from the InterPro Predicted Protein Domain Annotations dataset.
intraventricular block Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intraventricular block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bundle branch block Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bundle branch block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart block Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sinoatrial block Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sinoatrial block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
heart block, nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the heart block, nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
heart block, progressive, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the heart block, progressive, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
Right Bundle Branch Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Bundle Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trifascicular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trifascicular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Bundle-Branch Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Bundle-Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Incomplete Right Bundle Branch Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Incomplete Right Bundle Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prolonged Neuromuscular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prolonged Neuromuscular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bundle-Branch Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bundle-Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Posterior Fascicular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Posterior Fascicular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinoatrial Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinoatrial Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Anterior Fascicular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Anterior Fascicular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Heart Block With Broad Qrs Complexes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Heart Block With Broad Qrs Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart Block, Nonprogressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Block, Nonprogressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Familial Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Familial Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Av Block First Degree By Ecg Finding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Av Block First Degree By Ecg Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Av Block Second Degree By Ecg Finding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Av Block Second Degree By Ecg Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Block Vertebrae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Block Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Right Bundle Branch Block Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Right Bundle Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Heart Block Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
heart block Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the heart block phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sinoatrial block Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sinoatrial block phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bundle branch block Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bundle branch block phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intraventricular block Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intraventricular block phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Progressive familial heart block Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial heart block from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Right bundle branch block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Right bundle branch block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial heart block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Trifascicular block on electrocardiogram Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Trifascicular block on electrocardiogram phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dandy-Walker like malformation with atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset.
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.
atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrioventricular Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term atrioventricular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
atrioventricular node development Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular node development biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular bundle cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular bundle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular valve morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular node cell fate commitment Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular node cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular valve formation Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular valve formation biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular node cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular node cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular canal development Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular canal development biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular valve development Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular valve development biological process from the curated GO Biological Process Annotations 2015 dataset.
Atrioventricular conduction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Atrioventricular conduction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abnormal atrioventricular conduction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal atrioventricular conduction Gene Set From HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the atrioventricular valves Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the atrioventricular valves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal atrioventricular connection Gene Set From HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased atrioventricular cushion size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased atrioventricular cushion size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular node conduction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular node conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal septation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
biventricular, discordant atrioventricular connection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the biventricular, discordant atrioventricular connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent atrioventricular cushions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent atrioventricular cushions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular bundle conduction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular bundle conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
biventricular, ambiguous atrioventricular connection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the biventricular, ambiguous atrioventricular connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
unbalanced complete common atrioventricular canal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the unbalanced complete common atrioventricular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
common atrioventricular valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the common atrioventricular valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular cushion morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular cushion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin atrioventricular cushion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin atrioventricular cushion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular node morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular bundle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular valve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular valve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of atrioventricular cushion closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of atrioventricular cushion closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrioventricular valve regurgitation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrioventricular valve regurgitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal atrioventricular septum morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal atrioventricular septum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{atrioventricular septal defect, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrioventricular septal defect, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 5 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Atrioventricular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Defect Of Atrioventricular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Defect Of Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transitional Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transitional Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Common Atrioventricular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Common Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Reciprocating Tachycardia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Reciprocating Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Re-Entrant Atrioventricular Tachycardia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Re-Entrant Atrioventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anomalous Atrioventricular Excitation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anomalous Atrioventricular Excitation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Atrioventricular Conduction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Atrioventricular Conduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unbalanced Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unbalanced Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
atrioventricular valve morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular valve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular valve development Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular valve development biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular node cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular node cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular node development Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular node development biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular valve formation Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular valve formation biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular bundle cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular bundle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular node cell fate commitment Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular node cell fate commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
atrioventricular node cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the atrioventricular node cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal atrioventricular valve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular valve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular cushion morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular cushion morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
common atrioventricular valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the common atrioventricular valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent atrioventricular cushions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent atrioventricular cushions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin atrioventricular cushion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin atrioventricular cushion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular valve regurgitation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular valve regurgitation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of atrioventricular cushion closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of atrioventricular cushion closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased atrioventricular cushion size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased atrioventricular cushion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased atrioventricular cushion size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular septum morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular septum morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular cushion hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular cushion hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular node morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular node morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular node conduction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular node conduction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular bundle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal atrioventricular bundle conduction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrioventricular bundle conduction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
partial atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
biventricular, discordant atrioventricular connection Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the biventricular, discordant atrioventricular connection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
biventricular, ambiguous atrioventricular connection Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the biventricular, ambiguous atrioventricular connection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
balanced complete atrioventricular canal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the balanced complete atrioventricular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unbalanced complete atrioventricular canal, left dominant Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unbalanced complete atrioventricular canal, left dominant phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unbalanced complete common atrioventricular canal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unbalanced complete common atrioventricular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular node hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular node hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Atrioventricular canal cell_Heart_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Atrioventricular canal cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
atrioventricular valve morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular valve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular valve development Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular valve development biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular node cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular node cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular node development Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular node development biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular valve formation Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular valve formation biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular bundle cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular bundle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular node cell fate commitment Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular node cell fate commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
atrioventricular node cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the atrioventricular node cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
Atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrioventricular node Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Atrioventricular node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular conduction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atrioventricular conduction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, vitelliform, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Occult macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bietti crystalline corneoretinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thiel-Behnke corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reis-Bucklers' corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy, X-linked 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitelliform dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitelliform dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy Fuchs endothelial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schnyder crystalline corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONE DYSTROPHY 5, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy type 3A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, vitelliform, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy Type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Groenouw corneal dystrophy type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal epithelial dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi Muscular Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, gelatinous drop-like Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral muscular dystrophy 1a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, retinal, 1, North Carolina type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 8 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 7 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy Avellino type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, atypical vitelliform Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, concentric annular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, concentric annular from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 13 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Animal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Endothelial, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.
Macular Dystrophy, Retinal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.
Lattice corneal dystrophy type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Bullous Dystrophy, Hereditary Macular Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reflex Sympathetic Dystrophy from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Crystalline, of Schnyder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset.
Scleroatonic muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lisch Epithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, epithelial basement membrane Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.
MACULAR DYSTROPHY, RETINAL, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 9 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.
Doyne honeycomb retinal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.
Bietti Crystalline Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bietti Crystalline Dystrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.
OCCULT MACULAR DYSTROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OCCULT MACULAR DYSTROPHY from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.
Asphyxiating Thoracic Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Oculopharyngeal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fleck Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.
Retinal cone dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy, limb-girdle, type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset.
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitelliform Macular Dystrophy from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Congenital Stromal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
Choroidal dystrophy central areolar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Thiel-Behnke type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 12 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 11 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 10 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Newfoundland Rod-Cone Dystrophy from the curated CTD Gene-Disease Associations dataset.
Groenouw type I corneal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 15 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lattice Type IIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy of Bowman layer, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, corneal type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Lmna-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lattice corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitelliform macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitelliform macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal granular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal granular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reflex sympathetic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vulvar dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
occult macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fuchs' endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bietti crystalline corneoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuroaxonal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroaxonal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitreoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitreoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease granular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gelatinous droplike corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gelatinous droplike corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular corneal dystrophy. Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, oculopharyngeal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinitis pigmentosa; macular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; macular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs' endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs' endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lattice corneal dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recessive cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease recessive cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dystrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Fuchs's corneal dystrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
corneal dystrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease corneal dystrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
nail dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nail dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polymorphous posterior corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lattice corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the lattice corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macroreticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macroreticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the granular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
map-dot-fingerprint corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
speckled corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the speckled corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
crystalline corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the crystalline corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the choroidal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
marginal corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the marginal corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nodular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nodular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile epithelial corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mosaic corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the mosaic corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the punctate corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the reticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex Sympathetic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitelliform Macular Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitelliform Macular Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
nail dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nail dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
corneal dystrophy, schnyder type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.
fascioscapulohumeral muscular dystrophy 2, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
newfoundland rod-cone dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
bothnia retinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, megaconial type Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.
t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
occult macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract with late-onset corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2c Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, congenital stromal Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type iiia Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy, x-linked, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, gelatinous drop-like Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 6, 60177 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy, limb-girdle, type 2r Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
toenail dystrophy, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, rigid spine, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, epithelial basement membrane Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, merosin-positive Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2d Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2j Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.
hypotrichosis, congenital, with juvenile macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy and perceptive deafness Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy and perceptive deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, north carolina type Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.
tibial muscular dystrophy, tardive Gene Set From OMIM Gene-Disease Associations genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, reis-bucklers type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, patterned, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, thiel-behnke type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy with central cone involvement Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
choriodal dystrophy, central areolar 2 Gene Set From OMIM Gene-Disease Associations genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, endothelial, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 3, ar Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
limb-girdle muscular dystrophy, type 1g Gene Set From OMIM Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.
sorsby fundus dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sorsby fundus dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with rimmed vacuoles Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
bietti crystalline corneoretinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 6, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with epidermolysis bullosa simplex Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset.
vitelliform macular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vitelliform macular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 1, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
becker muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, groenouw type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
meesmann corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal fleck dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the corneal fleck dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
?cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 7, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital merosin-deficient Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal cone dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3b Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, avellino type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lisch epithelial Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lisch epithelial phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
Emery-Dreifuss muscular dystrophy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Bietti Crystalline Corneoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bietti Crystalline Corneoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
North Carolina Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease North Carolina Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obsolete Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obsolete Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Avellino Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Avellino Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy, Granular Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy, Granular in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Or Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Or Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiel-Behnke Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiel-Behnke Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eichsfeld Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eichsfeld Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lattice Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lattice Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne And Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne And Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Walker-Warburg Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Walker-Warburg Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fukuyama Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fukuyama Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Cervical Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Cervical Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Schnyder Crystalline Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Schnyder Crystalline Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymorphous Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Best Vitelliform Macular Dystrophy, Multifocal (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Best Vitelliform Macular Dystrophy, Multifocal (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ullrich Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ullrich Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reflex Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Limb Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Limb Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy, Tardive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy, Tardive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenintal Hereditary Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenintal Hereditary Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jeune Thoracic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jeune Thoracic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mosaic Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mosaic Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Type Ii (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy Type Ii (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Recurrent Erosion Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hereditary Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hereditary Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toenail Dystrophy, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Concentric Annular Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Concentric Annular Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Butterfly-Shaped Pigmentary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Butterfly-Shaped Pigmentary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patterned Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patterned Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marginal Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marginal Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intermediate Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intermediate Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe [Duchenne] Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe [Duchenne] Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy With Supernormal Rod Response Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy With Supernormal Rod Response in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occult Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occult Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmentary Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmentary Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Granular Dystrophy, Corneal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Granular Dystrophy, Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ocular Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ocular Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Sclerosing Bone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sclerosing Bone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Speckled Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Speckled Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pre-Descemet'S Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pre-Descemet'S Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bull'S Eye Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bull'S Eye Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pattern Dystrophy Of The Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pattern Dystrophy Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bothnia Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Newfoundland Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gelatinous Droplike Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gelatinous Droplike Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Basement Membrane Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Basement Membrane Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Groenouw Corneal Dystrophy Type I (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Groenouw Corneal Dystrophy Type I (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Punctate Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Punctate Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reis-Bucklers' Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reis-Bucklers' Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Salzmann Nodular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Salzmann Nodular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy Of Vulva Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy Of Vulva in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nodular Corneal Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nodular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nail dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nail dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Affected pathways in Duchenne muscular dystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Affected pathways in Duchenne muscular dystrophy pathway from the WikiPathways Pathways 2024 dataset.
Muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Emery-Dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Gelatinous drop-like corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gelatinous drop-like corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
epithelial-stromal TGFBI dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease epithelial-stromal TGFBI dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Epithelial and subepithelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Epithelial and subepithelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Lattice corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lattice corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital merosin-deficient muscular dystrophy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Meesmann corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Meesmann corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fundus dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fundus dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary retinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fuchs' endothelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fuchs' endothelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Corneal endothelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal endothelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Miyoshi muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy-dystroglycanopathy type A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy-dystroglycanopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Stromal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Stromal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital stromal corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital stromal corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease T-cell immunodeficiency, congenital alopecia, and nail dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Tibial muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Tibial muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bietti crystalline corneoretinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cone-rod dystrophy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cone dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cone dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuroaxonal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuroaxonal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fuchs' endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Doyne honeycomb retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitelliform macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitelliform macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
epithelial-stromal TGFBI dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease epithelial-stromal TGFBI dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lattice corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Emery-Dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Schnyder corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Schnyder corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital stromal corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital stromal corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Stromal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stromal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subepithelial mucinous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subepithelial mucinous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial and subepithelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial and subepithelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hypotrichosis with juvenile macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hypotrichosis with juvenile macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fleck corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fleck corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sorsby's fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sorsby's fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gelatinous drop-like corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gelatinous drop-like corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Meesmann corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Meesmann corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2S Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2S in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thiel-Behnke corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thiel-Behnke corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal dystrophy with leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal dystrophy with leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reflex sympathetic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bietti crystalline corneoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hereditary endothelial dystrophy of cornea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hereditary endothelial dystrophy of cornea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2M Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2M in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital merosin-deficient muscular dystrophy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megaconial type congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megaconial type congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lisch epithelial corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lisch epithelial corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal dystrophy-perceptive deafness syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy-perceptive deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior amorphous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior amorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reis-Bucklers corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reis-Bucklers corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial recurrent erosion dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial recurrent erosion dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type C8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type C8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Occult macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cone-rod dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cone-rod dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cone-rod dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cone-rod dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2X Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2X in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial basement membrane dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial basement membrane dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tibial muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tibial muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked Emery-Dreifuss muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked Emery-Dreifuss muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T-cell immunodeficiency, congenital alopecia, and nail dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondylometaphyseal dysplasia with cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2Q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vulvar dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulvar dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bothnia retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bothnia retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Newfoundland cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Newfoundland cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitreoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitreoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked Emery-Dreifuss muscular dystrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked Emery-Dreifuss muscular dystrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive Emery-Dreifuss muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive Emery-Dreifuss muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Harmonizome 3.0

atrioventricular block; myotonic dystrophy Gene Set

Electrocardiogram Atrioventricular Block Complete Heart Block Gene Set

Atrioventricular Block Gene Set

atrioventricular block Gene Set

atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set

third degree atrioventricular block Gene Set

first degree atrioventricular block Gene Set

atrioventricular block Gene Set

Atrioventricular Block Gene Set

atrioventricular block Gene Set

Complete Atrioventricular Block Gene Set

First Degree Atrioventricular Block Gene Set

Atrioventricular Block Gene Set

Second Degree Atrioventricular Block Gene Set

atrioventricular block Gene Set

second-degree atrioventricular block Gene Set

Atrioventricular block Gene Set

third-degree atrioventricular block Gene Set

first-degree atrioventricular block Gene Set

Mobitz type II atrioventricular block Gene Set

Atrioventricular block Gene Set

Third degree atrioventricular block Gene Set

First degree atrioventricular block Gene Set

Atrioventricular septal defect and common atrioventricular junction Gene Set

Myotonic Dystrophy Gene Set

myotonic dystrophy type 1 Gene Set

myotonic dystrophy type 1 Gene Set

myotonic dystrophy type 2 Gene Set

machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set

myotonic dystrophy type 1 Gene Set

chromosome disorders; myotonic dystrophy Gene Set

carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set

fibromyalgia; myotonic dystrophy Gene Set

myotonic dystrophy Gene Set

Myotonic Dystrophy Gene Set

Myotonic dystrophy protein kinase, coiled coil Gene Set

myotonic dystrophy 2 Gene Set

myotonic dystrophy 1 Gene Set

myotonic dystrophy type1 Gene Set

Myotonic Dystrophy Gene Set

Congenital Myotonic Dystrophy Gene Set

Myotonic dystrophy type 1 Gene Set

Myotonic dystrophy type 1 Gene Set

Myotonic dystrophy type 2 Gene Set

Steinert myotonic dystrophy syndrome Gene Set

Myotonic dystrophy Gene Set

myotonic disease Gene Set

myotonic disease Gene Set

myotonic disorders Gene Set

myotonic Gene Set

emg: myotonic runs Gene Set

Myotonic Disorders Gene Set

Emg: Myotonic Runs Gene Set

Emg: Myotonic Discharges Gene Set

Myotonic disease Gene Set

Myotonic disease Gene Set

Myotonic cataract Gene Set

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

Heart block, nonprogressive Gene Set

Progressive familial heart block type 1A Gene Set

Progressive familial heart block type 1B Gene Set

pluronic block copolymer p85 Gene Set

Heart Block Gene Set

Sinoatrial Block Gene Set

Bundle-Branch Block Gene Set

PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set

Progressive Familial Heart Block, Type Ib Gene Set

congenital heart block Gene Set

right bundle branch block Gene Set

progressive av-block and anomalous venous return Gene Set

autoimmune-associated congenital heart block. Gene Set

block Gene Set

heart block Gene Set

left bundle branch block Gene Set

left anterior fascicular block Gene Set

complete heart block with broad rs complexes Gene Set

heart block Gene Set

block vertebrae Gene Set

bundle branch block Gene Set