Familial Cold Autoinflammatory Syndrome

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Results for "Familial Cold Autoinflammatory Syndrome": 55 genes, 1004 gene sets

Name
CSDC2 Gene cold shock domain containing C2, RNA binding Predicted to enable mRNA 3'-UTR binding activity. Predicted to be involved in regulation of mRNA stability. Predicted to be located in nucleus. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
CIRBP Gene cold inducible RNA binding protein Enables mRNA 3'-UTR binding activity and small ribosomal subunit rRNA binding activity. Involved in mRNA stabilization; positive regulation of translation; and response to UV. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]
CSDE1 Gene cold shock domain containing E1, RNA-binding Enables RISC complex binding activity; RNA stem-loop binding activity; and lncRNA binding activity. Involved in IRES-dependent viral translational initiation; regulation of gene expression; and stress granule assembly. Located in Golgi apparatus; cytosol; and plasma membrane. Part of CRD-mediated mRNA stability complex and mCRD-mediated mRNA stability complex. [provided by Alliance of Genome Resources, Mar 2025]
AAA1 Gene aortic aneurysm, familial* abdominal 1*
AAA3 Gene Aneurysm, familial* abdominal 3*
AAA2 Gene Aortic aneurysm, familial* abdominal 2*
AAA4 Gene Aortic aneurysm, familial* abdominal, 4*
ETL6 Gene Epilepsy, familial* temporal lobe, 6*
RCM2 Gene cardiomyopathy, familial* restrictive, 2*
ATFB8 Gene Atrial fibrillation, familial, 8
HNFJ3 Gene Hyperuricemic nephropathy, familial* juvenile, 3*
GPSC Gene gliosis, familial* progressive subcortical*
BHD Gene Beukes familial* hip dysplasia*
FAME4 Gene Epilepsy, familial* adult myoclonic, 4*
FAME3 Gene Epilepsy, familial* adult myoclonic, 3*
PFHB2 Gene Progressive familial* heart block, type II*
BFIS1 Gene benign familial* infantile convulsions*
HBN1 Gene Progressive familial* heart block, type I, locus 1*
ETL2 Gene epilepsy, familial* temporal lobe*
FHII Gene Hyperaldosteronism, familial, type II
FCMTE2 Gene familial cortical myoclonic tremor with epilepsy 2
FCMTE1 Gene familial cortical myoclonic tremor with epilepsy 1
GLM4 Gene Glioma, familial, 1
PSHK2 Gene Pseudohyperkalemia, familial, 2, due to red cell leak
VVS Gene Syncope, familial* vasovagal*
BFIS4 Gene Convulsions, benign familial* infantile, 4*
ATFB1 Gene Atrial fibrillation, familial* 1*
ATFB2 Gene familial atrial fibrillation 2
SXI2 Gene X inactivation, familial* skewed, 2*
BFIC2 Gene Benign familial* infantile convulsions-2*
FMTLE Gene Epilepsy, familial* mesial temporal lobe*
STUT3 Gene Stuttering, familial* persistent, 3*
STUT2 Gene Stuttering, familial* persistent 2*
STUT1 Gene Stuttering, familial* persistent 1*
STUT4 Gene Stuttering, familial* persistent, 4*
BRCD1 Gene cancer, familial, with in vitro radioresistance
MGR2 Gene Migraine, familial* typical, susceptibility to*
MGR3 Gene Migraine, familial, with or without aura, susceptibility to
MFT2 Gene Trichoepithelioma, multiple familial, 2
FEB9 Gene Febrile convulsions, familial, 9
ATFB5 Gene Atrial fibrillation, familial, 5
HTGS Gene Hypertriglyceridemia, familial
DIP Gene interstitial pneumonitis, desquamative, familial
CMH21 Gene Cardiomyopathy, familial* hypertrophic, 21*
CANDF1 Gene candidiasis, familial* 1*
ATPLS Gene antiphospholipid syndrome, familial
EOS Gene eosinophilia, familial
FEB10 Gene Febrile convulsions, familial, 10
LVNC2 Gene noncompaction of left ventricular myocardium, familial* isolated, autosomal dominant 2*
THCYTX Gene Thrombocytosis, familial* X-linked*
CMS1A1 Gene myasthenia gravis, familial* infantile, 1*
BPPV Gene vestibulopathy, familial
AAT2 Gene Aortic aneurysm, familial* thoracic 2*
AAT1 Gene Aortic aneurysm, familial* thoracic 1*
NKCD Gene Natural killer cell deficiency, familial* isolated*
Familial Cold Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cold Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial cold autoinflammatory syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial cold autoinflammatory syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cold autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Familial Cold Autoinflammatory Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
?familial cold autoinflammatory syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ?familial cold autoinflammatory syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold autoinflammatory syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold autoinflammatory syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial cold autoinflammatory syndrome 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial cold autoinflammatory syndrome 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial cold autoinflammatory syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoinflammatory Syndrome, Familial, Behcet-Like Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoinflammatory Syndrome, Familial, Behcet-Like in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Behcet-like autoinflammatory syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial Behcet-like autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
familial cold-induced inflammatory syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial cold urticaria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial Cold Urticaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cold Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proteasome-Associated Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proteasome-Associated Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monogenic Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monogenic Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Otulin-Related Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Otulin-Related Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
proteosome-associated autoinflammatory syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease proteosome-associated autoinflammatory syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease proteasome-associated autoinflammatory syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteasome-associated autoinflammatory syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteasome-associated autoinflammatory syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proteasome-associated autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proteasome-associated autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proteosome-associated autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proteosome-associated autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Periodic fever-infantile enterocolitis-autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever-infantile enterocolitis-autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cold-induced sweating syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cold-induced sweating syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cold-Induced Sweating Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cold-Induced Sweating Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
cold-induced sweating syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cold-induced sweating syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cold-induced sweating syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cold-induced sweating syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Cold-Induced Sweating Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cold-Induced Sweating Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crisponi/Cold-Induced Sweating Syndrome 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Crisponi/Cold-Induced Sweating Syndrome 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
cold-induced sweating syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease cold-induced sweating syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cold-induced sweating syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cold-induced sweating syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cold-induced sweating syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cold-induced sweating syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cold-induced sweating syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cold-induced sweating syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cold-induced sweating syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cold-induced sweating syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cold-induced sweating syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cold-induced sweating syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe mucosal involvement Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe mucosal involvement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hereditary Autoinflammatory Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Autoinflammatory Diseases from the curated CTD Gene-Disease Associations dataset.
autoinflammatory Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term autoinflammatory in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Hereditary Autoinflammatory Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Autoinflammatory Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Autoinflammatory Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoinflammatory Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoinflammatory Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoinflammatory Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoinflammatory disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammatory disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Common Cold Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Common Cold from the curated CTD Gene-Disease Associations dataset.
common cold Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease common cold in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
common cold; otitis media; picornaviridae infections Gene Set From GAD Gene-Disease Associations genes associated with the disease common cold; otitis media; picornaviridae infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
common cold; Gene Set From GAD Gene-Disease Associations genes associated with the disease common cold; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allergies; common cold Gene Set From GAD Gene-Disease Associations genes associated with the disease allergies; common cold in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cold Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cold in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cold acclimation Gene Set From GO Biological Process Annotations 2015 genes participating in the cold acclimation biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to cold Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to cold biological process from the curated GO Biological Process Annotations 2015 dataset.
response to cold Gene Set From GO Biological Process Annotations 2015 genes participating in the response to cold biological process from the curated GO Biological Process Annotations 2015 dataset.
Blood pressure measurement (cold pressor test) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
cold-induced hand cramps Gene Set From HPO Gene-Disease Associations genes associated with the cold-induced hand cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cold-induced muscle cramps Gene Set From HPO Gene-Disease Associations genes associated with the cold-induced muscle cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Common Cold Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Common Cold phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cold-shock protein, DNA-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cold-shock protein, DNA-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cold shock protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cold shock protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cold-shock conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cold-shock conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Common Cold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Common Cold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cold Hypersensitivity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cold Hypersensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cold Hemagglutinin Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cold Hemagglutinin Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urticaria Due To Cold And Heat Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold And Heat in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urticaria Due To Cold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cold Paroxysmal Hemoglobinuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cold Paroxysmal Hemoglobinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Cold Nodule Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Cold Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cold Symptoms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cold Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cold-Induced Hand Cramps Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cold-Induced Hand Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cold-Induced Muscle Cramps Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cold-Induced Muscle Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cold Paresis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cold Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cold-Sensitive Myotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cold-Sensitive Myotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Feeling Cold Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Feeling Cold in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
negative regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to cold Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to cold biological process from the curated GO Biological Process Annotations 2023 dataset.
detection of cold stimulus involved in thermoception Gene Set From GO Biological Process Annotations 2023 genes participating in the detection of cold stimulus involved in thermoception biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cold acclimation Gene Set From GO Biological Process Annotations 2023 genes participating in the cold acclimation biological process from the curated GO Biological Process Annotations 2023 dataset.
sensory perception of cold stimulus Gene Set From GO Biological Process Annotations 2023 genes participating in the sensory perception of cold stimulus biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to cold Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to cold biological process from the curated GO Biological Process Annotations 2025 dataset.
detection of cold stimulus involved in thermoception Gene Set From GO Biological Process Annotations 2025 genes participating in the detection of cold stimulus involved in thermoception biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
cold acclimation Gene Set From GO Biological Process Annotations 2025 genes participating in the cold acclimation biological process from the curated GO Biological Process Annotations 2025 dataset.
cold-induced thermogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the cold-induced thermogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
sensory perception of cold stimulus Gene Set From GO Biological Process Annotations 2025 genes participating in the sensory perception of cold stimulus biological process from the curated GO Biological Process Annotations 2025 dataset.
Common cold Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Common cold in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cold sores Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cold sores phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Blood pressure measurement (cold pressor test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
hemolysis of donated blood (cold-storage) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the hemolysis of donated blood (cold-storage) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial antiphospholipid syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
familial nephrotic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; hyper-igd syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; hyper-igd syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carpal tunnel syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep phase syndrome, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
cutaneous telangiectasia and cancer syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
?antiphospholipid syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the ?antiphospholipid syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep-phase syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial Atypical Mole Melanoma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Mole Melanoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Sick Sinus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Sick Sinus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Guillain-Barre Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Guillain-Barre Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cutaneous Telangiectasia And Cancer Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Telangiectasia And Cancer Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hemolytic Uremic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Hemolytic Uremic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Charge Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Charge Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Factor Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Antiphospholipid Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dandy-Walker Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelocytic Leukemia-Like Syndrome, Familial, Chronic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelocytic Leukemia-Like Syndrome, Familial, Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carpal Tunnel Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carpal Tunnel Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Scaphocephaly Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Familial Scaphocephaly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Familial chylomicronemia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial chylomicronemia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial nephrotic syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial nephrotic syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial chylomicronemia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial chylomicronemia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial nephrotic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial woolly hair syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial woolly hair syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial episodic pain syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic steroid-resistant nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial scaphocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial scaphocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial cardiofaciocutaneous syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cardiofaciocutaneous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial Atypical Hemolytic-Uremic Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Atypical Hemolytic-Uremic Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial episodic pain syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial episodic pain syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial steroid-resistant nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial sick sinus syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sick sinus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Familial Mediterranean fever Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, hyperphosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemic nephropathy, familial juvenile, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cancer of breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial aortopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital arthropathy-brachydactyly, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial visceral amyloidosis, Ostertag type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia familial British Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
familial hyperinsulinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia familial 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paroxysmal familial ventricular fibrillation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypercholesterolemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hidradenitis suppurativa, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia, familial Danish Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria 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.
Familial dysautonomia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial febrile seizures 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial exudative vitreoretinopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial colorectal cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porphyria cutanea tarda Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonus, familial cortical Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Migraine, familial basilar Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholanemia, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypokalemia-hypomagnesemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenia, limb-girdle, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular fibrillation, paroxysmal familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial erythrocytosis, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperlipidemia, familial combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial amyloid polyneuropathy, Iowa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, familial adult myoclonic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial myxoma, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial juvenile gout Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypobetalipoproteinemia, familial, associated with apob32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 3 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, normophosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd8 deficiency, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial atypical mycobacteriosis, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperthyroxinemia, familial dysalbuminemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 5 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial pulmonary capillary hemangiomatosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoalphalipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal hypouricemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoplastic, glomerulocystic kidney Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Aneurysm, Familial Abdominal 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.
Familial myelofibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset.
Nephronophthisis, familial juvenile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.
Eosinophilia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, familial visceral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.
STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.
Dementia, familial British Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
CD8 Deficiency, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.
Insomnia, Fatal Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset.
Familial dermographism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperthyroidism, Familial Gestational Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Migraine, Familial Hemiplegic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.
Cancer, Familial, with In Vitro Radioresistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Hypoparathyroidism familial isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hidradenitis suppurativa, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.
Dementia, familial Danish Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.
Familial medullary thyroid carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.
Interstitial Pneumonitis, Desquamative, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.
Cirrhosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Familial Partial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Keratoacanthoma familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.
Familial Wilms tumor 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Atrial fibrillation, familial 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.
Meningioma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Adult Myoclonic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.
Prostate cancer, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital 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.
Aortic Aneurysm, Familial Thoracic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
Hyperthyroxinemia, Familial Dysalbuminemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial cylindromatosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Hyperaldosteronism, Familial, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Atrial myxoma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Normophosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.
Periodic fever, familial, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.
Familial schizencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.
Neurofibromatosis, Familial Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.
Reticuloendotheliosis, familial, with eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.
MITRAL VALVE PROLAPSE, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL 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.
Familial dilated cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Thymoma, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.
Familial apoceruloplasmin deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.
HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Amyloid Neuropathies, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.
CANDIDIASIS, FAMILIAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Stuttering, Familial Persistent 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Temporal Lobe, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypertriglyceridemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial combined hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal familial insomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial mediterranean fever Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial glomangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypercholesterolemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial partial lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial visceral amyloidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal papillary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial or sporadic prostate cancer. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b100. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies; amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset familial alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdomen, acute; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysbetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease (familial) Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set From GAD Gene-Disease Associations genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial premature myocardial infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset of familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b-100 in a chinese man Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; familial mediterranean fever; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial male-limited precocious puberty. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidaemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial early onset psoriasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypobetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypobetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy in a hungarian family. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in a hungarian family. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease familial melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypocalciuric hypercalcemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hyperinsulinism. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hyperinsulinism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial glucocorticoid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease familial glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial partial lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial partial lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial liver adenomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial liver adenomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea; familial mediterranean fever; pain; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertrophic cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; atherosclerosis; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; atherosclerosis; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial exudative vitreoretinopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial exudative vitreoretinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysautonomia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysautonomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial alzheimer's disease associated Gene Set From GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
greenland familial cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial diabetes insipidus Gene Set From GAD Gene-Disease Associations genes associated with the disease familial diabetes insipidus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial erythrocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial erythrocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial bronchiectasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial bronchiectasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial non-ret c cell hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertension of early onset. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term familial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Parkinson's disease (familial) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
familial hypertriglyceridemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial atrial fibrillation Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial predisposition Gene Set From HPO Gene-Disease Associations genes associated with the familial predisposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperlipidemia, Familial Combined phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paralyses, Familial Periodic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paralyses, Familial Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Familial Mediterranean Fever Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Familial Mediterranean Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lipodystrophy, Familial Partial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lipodystrophy, Familial Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloidosis, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysautonomia, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysautonomia, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloid Neuropathies, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloid Neuropathies, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Insomnia, Fatal Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Insomnia, Fatal Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial focal, with variable foci Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, familial primary Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrial fibrillation, familial, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
digital arthropathy-brachydactyly, familial Gene Set From OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease 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.
migraine, familial basilar Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 8 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 9 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
insomnia, fatal familial Gene Set From OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dysautonomia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined hyperlipidemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the combined hyperlipidemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypobetalipoproteinemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hypobetalipoproteinemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3a Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial danish Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial danish phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[igg receptor i, phagocytic, familial deficiency of] Gene Set From OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
?epilepsy, familial adult myoclonic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
?candidiasis, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ?candidiasis, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 22 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary thyroid carcinoma, familial Gene Set From OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, paroxysmal familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
endometrial cancer, familial Gene Set From OMIM Gene-Disease Associations genes associated with the endometrial cancer, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial, nonspecific Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
amyloidosis, familial visceral Gene Set From OMIM Gene-Disease Associations genes associated with the amyloidosis, familial visceral phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, familial benign Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, benign familial Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial british Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial british phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudohyperkalemia, familial, 2, due to red cell leak Gene Set From OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, limb-girdle, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, limb-girdle, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[erythrocytosis, familial, 1] Gene Set From OMIM Gene-Disease Associations genes associated with the [erythrocytosis, familial, 1] phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, familial typical, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, familial typical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary hypertension, familial primary, 1, with or without hht Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia, familial, due to decreased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
cylindromatosis, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cylindromatosis, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskinesia, familial, with facial myokymia Gene Set From OMIM Gene-Disease Associations genes associated with the dyskinesia, familial, with facial myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, familial isolated Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, familial isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
gastrointestinal stromal tumor, familial Gene Set From OMIM Gene-Disease Associations genes associated with the gastrointestinal stromal tumor, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{aneurysm, familial abdominal 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {aneurysm, familial abdominal 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
x inactivation, familial skewed, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the x inactivation, familial skewed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 5, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholanemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholanemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 4, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 4, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{prostate cancer, familial, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {prostate cancer, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
familial mediterranean fever, ar Gene Set From OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial adult myoclonic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cd8 deficiency, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cd8 deficiency, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set From OMIM Gene-Disease Associations genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{coronary artery disease in familial hypercholesterolemia, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {coronary artery disease in familial hypercholesterolemia, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombotic thrombocytopenic purpura, familial Gene Set From OMIM Gene-Disease Associations genes associated with the thrombotic thrombocytopenic purpura, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
osteolysis, familial expansile Gene Set From OMIM Gene-Disease Associations genes associated with the osteolysis, familial expansile phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, infantile, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
[gamma-glutamyltransferase, familial high serum] Gene Set From OMIM Gene-Disease Associations genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectopia lentis, familial Gene Set From OMIM Gene-Disease Associations genes associated with the ectopia lentis, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
platelet disorder, familial, with associated myeloid malignancy Gene Set From OMIM Gene-Disease Associations genes associated with the platelet disorder, familial, with associated myeloid malignancy phenotype from the curated OMIM Gene-Disease Associations dataset.
neurofibromatosis, familial spinal Gene Set From OMIM Gene-Disease Associations genes associated with the neurofibromatosis, familial spinal phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cell carcinoma, papillary, 1, familial and somatic Gene Set From OMIM Gene-Disease Associations genes associated with the renal cell carcinoma, papillary, 1, familial and somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
tumoral calcinosis, familial, normophosphatemic Gene Set From OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, familial, normophosphatemic phenotype from the curated OMIM Gene-Disease Associations dataset.
{hyperlipidemia, familial combined, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hyperlipidemia, familial combined, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
tumoral calcinosis, hyperphosphatemic, familial Gene Set From OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, hyperphosphatemic, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial mediterranean fever, ad Gene Set From OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, familial, due to ttf-1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
{meningioma, familial, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {meningioma, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, myoclonic, familial adult, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
?lipodystrophy, familial partial, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, familial partial, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalciuric hypercalcemia, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
periodic fever, familial Gene Set From OMIM Gene-Disease Associations genes associated with the periodic fever, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperfibrinolysis, familial, due to increased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperthyroidism, familial gestational Gene Set From OMIM Gene-Disease Associations genes associated with the hyperthyroidism, familial gestational phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease 1, familial Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease 1, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperproinsulinemia, familial, with or without diabetes Gene Set From OMIM Gene-Disease Associations genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.
vestibulopathy, familial Gene Set From OMIM Gene-Disease Associations genes associated with the vestibulopathy, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
eosinophilia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the eosinophilia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
x-inactivation, familial skewed Gene Set From OMIM Gene-Disease Associations genes associated with the x-inactivation, familial skewed phenotype from the curated OMIM Gene-Disease Associations dataset.
convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set From OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonus, familial cortical Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial (Fpah) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial (Fpah) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Alzheimer Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Alzheimer Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lichen Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lichen Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Glucocorticoid Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Cancer, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hdl Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hdl Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypercholesterolemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypercholesterolemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoalphalipoproteinemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoalphalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuchal Bleb, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuchal Bleb, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Exudative Vitreoretinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Exudative Vitreoretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mediterranean Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Intrahepatic Cholestasis Of Pregnancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Intrahepatic Cholestasis Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Creutzfeldt-Jakob Disease, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Creutzfeldt-Jakob Disease, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Periodic Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Periodic Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Gastric Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Gastric Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pseudohyperkalemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pseudohyperkalemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Familial Insomnia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Familial Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoadrenocorticism, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoadrenocorticism, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thrombocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Osteochondritis Dissecans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Osteochondritis Dissecans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Neurocardiogenic Syncope Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Neurocardiogenic Syncope in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Vesicoureteral Reflux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Vesicoureteral Reflux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Pemphigus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemic Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysautonomia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paroxysmal Familial Ventricular Fibrillation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paroxysmal Familial Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hematuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hematuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichoepitheliomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Epilepsies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Epilepsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thrombotic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Ectopia Lentis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Ectopia Lentis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dyskinesia, Familial, With Facial Myokymia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dyskinesia, Familial, With Facial Myokymia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dermographism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dermographism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Aplasia Of The Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Aplasia Of The Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Partial Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Adenomatous Polyposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Adenomatous Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperaldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Ductus Arteriosus Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Ductus Arteriosus Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acromegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acromegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Non-Medullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Somatotrophinoma, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Somatotrophinoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Intestinal Polyposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Danish Type Familial Amyloid Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Danish Type Familial Amyloid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lcat Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lcat Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Juvenile Parkinsonism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Juvenile Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypobetalipoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypobetalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Chondrocalcinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Chondrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Platelet Disorder, Familial, With Associated Myeloid Malignancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Platelet Disorder, Familial, With Associated Myeloid Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gigantiform Cementoma, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gigantiform Cementoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Nonmedullary Thyroid Gland Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Medullary Thyroid Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Medullary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Multiple Mole-Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dementia, Familial Danish Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dementia, Familial Danish in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperalphalipoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperalphalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lipoprotein Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lipoprotein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Apolipoprotein C-Ii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Apolipoprotein C-Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Testicular Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Motor Neuron Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cervical Artery Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cervical Artery Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Erythrocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Erythrocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Collagenosis, Familial Reactive Perforating Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Collagenosis, Familial Reactive Perforating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Tremor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Adult Familial Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Adult Familial Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hemiplegic Migraine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemiplegic Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Migraine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Alcoholism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Alcoholism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Central Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholanemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Renal Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Nonmedullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dermatitis Herpetiformis, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dermatitis Herpetiformis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Colorectal Camcer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Colorectal Camcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Cancer, Familial Male Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial Male in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Malignant Neoplasm Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Testotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hematuria, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Ventricular Tachycardia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Psoriasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Psoriasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pityriasis Rubra Pilaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pityriasis Rubra Pilaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Candidiasis, Familial, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Candidiasis, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Cavernous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Cavernous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Chronic Lymphocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Chronic Lymphocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cd8 Deficiency, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cd8 Deficiency, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Malignant Melanoma Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Melanoma Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Retinoblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Retinoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Infantile Myasthenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Convulsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Schizencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Schizencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Vascular Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Vascular Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Apoceruloplasmin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Apoceruloplasmin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Mesial Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Lipomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypoaldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypoaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mitral Valve Prolapse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mitral Valve Prolapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticuloendotheliosis, Familial, With Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticuloendotheliosis, Familial, With Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Epilepsy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Epilepsy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dyshormonogenetic Goiter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dyshormonogenetic Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thyroid Dyshormonogenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thyroid Dyshormonogenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hidradenitis Suppurativa, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hidradenitis Suppurativa, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Polycythemia Vera Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Polycythemia Vera in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lambdoid Synostosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lambdoid Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Premature Ovarian Failure, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Premature Ovarian Failure, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypophosphatemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Trichomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Trichomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acanthosis Nigricans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichodiscomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Spontaneous Pneumothorax Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Spontaneous Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Restrictive Cardiomyopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Restrictive Cardiomyopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acute Myeloid Leukemia With Mutated Cebpa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia With Mutated Cebpa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Bicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophia Maculosa Varioliformis Cutis, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophia Maculosa Varioliformis Cutis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Familial Brain Calcification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Familial Brain Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperekplexia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperekplexia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevi Flammei, Familial Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperpotassemia And Hypertension, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperpotassemia And Hypertension, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eunuchoidism, Familial Hypogonadotropic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eunuchoidism, Familial Hypogonadotropic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Extrahepatic Biliary Atresia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Porphyria Cutanea Tarda Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Porphyria Cutanea Tarda in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Renal Hypouricemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Renal Hypouricemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Adenomas, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Encephalopathy With Neuroserpin Inclusion Bodies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Encephalopathy With Neuroserpin Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Immunoglobulin A Nephropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Immunoglobulin A Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mastocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mastocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastrointestinal Stromal Tumor, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Stromal Tumor, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Hyper And Hypopigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Hyper And Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Obesity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Natural Killer Cell Deficiency, Familial Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Natural Killer Cell Deficiency, Familial Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Incomplete Male Pseudohermaphroditism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Incomplete Male Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mediterranean Fever, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Navajo Familial Neurogenic Arthropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Navajo Familial Neurogenic Arthropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypodontia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypodontia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Waldenstrom'S Macroglobulinaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Waldenstrom'S Macroglobulinaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Ebstein'S Anomaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Ebstein'S Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acoustic Neuroma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acoustic Neuroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Non-Neuropathic Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Neuropathic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Retina, Familial Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Retina, Familial Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrial Myxoma, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrial Myxoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperprolactinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperprolactinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Harmonizome 3.0

CSDC2 Gene

CIRBP Gene

CSDE1 Gene

AAA1 Gene

AAA3 Gene

AAA2 Gene

AAA4 Gene

ETL6 Gene

RCM2 Gene

ATFB8 Gene

HNFJ3 Gene

GPSC Gene

BHD Gene

FAME4 Gene

FAME3 Gene

PFHB2 Gene

BFIS1 Gene

HBN1 Gene

ETL2 Gene

FHII Gene

FCMTE2 Gene

FCMTE1 Gene

GLM4 Gene

PSHK2 Gene

VVS Gene

BFIS4 Gene

ATFB1 Gene

ATFB2 Gene

SXI2 Gene

BFIC2 Gene

FMTLE Gene

STUT3 Gene

STUT2 Gene

STUT1 Gene

STUT4 Gene

BRCD1 Gene

MGR2 Gene

MGR3 Gene

MFT2 Gene

FEB9 Gene

ATFB5 Gene

HTGS Gene

DIP Gene

CMH21 Gene

CANDF1 Gene

ATPLS Gene

EOS Gene

FEB10 Gene

LVNC2 Gene

THCYTX Gene

CMS1A1 Gene

BPPV Gene

AAT2 Gene

AAT1 Gene

NKCD Gene

Familial Cold Autoinflammatory Syndrome Gene Set

Familial cold autoinflammatory syndrome Gene Set

Familial cold autoinflammatory syndrome Gene Set

Familial cold autoinflammatory syndrome Gene Set

FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set

Familial Cold Autoinflammatory Syndrome 2 Gene Set

?familial cold autoinflammatory syndrome 4 Gene Set

familial cold autoinflammatory syndrome 3 Gene Set

familial cold autoinflammatory syndrome 2 Gene Set

Familial cold autoinflammatory syndrome 3 Gene Set

Familial cold autoinflammatory syndrome 2 Gene Set

Familial cold autoinflammatory syndrome 4 Gene Set

Familial cold autoinflammatory syndrome 3 Gene Set

Familial cold autoinflammatory syndrome 1 Gene Set

Autoinflammatory Syndrome, Familial, Behcet-Like Gene Set

Familial Behcet-like autoinflammatory syndrome Gene Set

familial cold-induced inflammatory syndrome 1 Gene Set

Familial cold urticaria Gene Set

Familial Cold Urticaria Gene Set

hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome Gene Set

Autoinflammatory Syndrome Gene Set

Proteasome-Associated Autoinflammatory Syndrome Gene Set

Monogenic Autoinflammatory Syndrome Gene Set

Otulin-Related Autoinflammatory Syndrome Gene Set