Name

CTD Gene-Disease Associations Dataset

From Comparative Toxicogenomics Database

Disease-gene interactions from manually curated literature

DISEASES Curated Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Disease gene evidence scores by manual literature curation

DISEASES Experimental Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Disease gene evidence scores by integrating experimental data (GWAS)

DISEASES Text-mining Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Gene-disease co-occurrence scores from text-mining biomedical abstracts

GAD Gene-Disease Associations Dataset

From Genetic Association Database

Gene-disease associations curated from genetic association studies

GAD High Level Gene-Disease Associations Dataset

From Genetic Association Database

Gene-disease associations curated from genetic association studies

GWASdb SNP-Disease Associations Dataset

From GWASdb

SNP-disease association p-values curated from published GWAS

HPO Gene-Disease Associations Dataset

From Human Phenotype Ontology

Phenotype-causing gene mutations of human phenotypes from disease knowledgebases

OMIM Gene-Disease Associations Dataset

From Online Mendelian Inheritance in Man

Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications

PhosphoSitePlus Phosphosite-Disease Associations Dataset

From PhosphoSitePlus

Disease-phosphosite associations curated from literature

DisGeNET Gene-Disease Associations Dataset

From DisGeNET

Gene-disease associations sourced from curated repositories, GWAS catalogues, animal models and the scientific literature

DISEASES Curated Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Disease gene evidence scores by manual literature curation

DISEASES Experimental Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Disease gene evidence scores by integrating experimental data (GWAS)

DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Gene-disease co-occurrence scores from text-mining biomedical abstracts

FAT3 Gene

FAT atypical cadherin 3

Predicted to enable calcium ion binding activity. Predicted to be involved in cell-cell adhesion. Predicted to act upstream of or within generation of neurons; negative regulation of dendrite development; and retina layer formation. Predicted to be located in dendrite and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

FAT2 Gene

FAT atypical cadherin 2

This gene is the second identified human homolog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has two epidermal growth factor (EGF)-like repeats and one laminin G domain. This protein most likely functions as a cell adhesion molecule, controlling cell proliferation and playing an important role in cerebellum development. [provided by RefSeq, Jul 2008]

FAT1 Gene

FAT atypical cadherin 1

This gene is an ortholog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has five epidermal growth factor (EGF)-like repeats and one laminin A-G domain. This gene is expressed at high levels in a number of fetal epithelia. Its product probably functions as an adhesion molecule and/or signaling receptor, and is likely to be important in developmental processes and cell communication. Transcript variants derived from alternative splicing and/or alternative promoter usage exist, but they have not been fully described. [provided by RefSeq, Jul 2008]

FAT1P1 Gene

FAT atypical cadherin 1 pseudogene 1

PEAK1 Gene

pseudopodium-enriched atypical kinase 1

This gene encodes a non-receptor tyrosine kinase that is a member of the new kinase family three (NFK3) family. In migrating cells, the encoded protein is associated with the actin cytoskeleton and focal adhesions and promotes developing focal adhesion elongation. This protein may play a role in the regulation of cell migration, proliferation and cancer metastasis. [provided by RefSeq, Mar 2014]

ACKR4 Gene

atypical chemokine receptor 4

The protein encoded by this gene is a member of the G protein-coupled receptor family, and is a receptor for C-C type chemokines. This receptor has been shown to bind dendritic cell- and T cell-activated chemokines including CCL19/ELC, CCL21/SLC, and CCL25/TECK. A pseudogene of this gene is found on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2013]

ACKR1 Gene

atypical chemokine receptor 1 (Duffy blood group)

The protein encoded by this gene is a glycosylated membrane protein and a non-specific receptor for several chemokines. The encoded protein is the receptor for the human malarial parasites Plasmodium vivax and Plasmodium knowlesi. Polymorphisms in this gene are the basis of the Duffy blood group system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACKR2 Gene

atypical chemokine receptor 2

This gene encodes a beta chemokine receptor, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. Chemokines and their receptor-mediated signal transduction are critical for the recruitment of effector immune cells to the inflammation site. This gene is expressed in a range of tissues and hemopoietic cells. The expression of this receptor in lymphatic endothelial cells and overexpression in vascular tumors suggested its function in chemokine-driven recirculation of leukocytes and possible chemokine effects on the development and growth of vascular tumors. This receptor appears to bind the majority of beta-chemokine family members; however, its specific function remains unknown. This gene is mapped to chromosome 3p21.3, a region that includes a cluster of chemokine receptor genes. [provided by RefSeq, Jul 2008]

ACKR3 Gene

atypical chemokine receptor 3

This gene encodes a member of the G-protein coupled receptor family. Although this protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP), it is now considered to be an orphan receptor, in that its endogenous ligand has not been identified. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas. [provided by RefSeq, Jul 2008]

VMD1 Gene

vitelliform macular dystrophy, atypical

FAT4 Gene

FAT atypical cadherin 4

The protein encoded by this gene is a member of the protocadherin family. This gene may play a role in regulating planar cell polarity (PCP). Studies in mice suggest that loss of PCP signaling may cause cystic kidney disease, and mutations in this gene have been associated with Van Maldergem Syndrome 2. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Mar 2014]

ACKR5 Gene

atypical chemokine receptor 5

NOAZFP Gene

nucleolar atypical zinc finger

Predicted to enable metal ion binding activity. Located in chromosome, centromeric region; midbody; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025]

Atypical Inclusion-Body Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Inclusion-Body Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Microvillus inclusion disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microvillus inclusion disease from the curated CTD Gene-Disease Associations dataset.

microvillus inclusion disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the microvillus inclusion disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Microvillus Inclusion Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Microvillus Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neuronal Intranuclear Inclusion Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neuronal Intranuclear Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Microvillus inclusion disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Microvillus inclusion disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Microvillus inclusion disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Microvillus inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neuronal intranuclear inclusion disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neuronal intranuclear inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

atypical sinopulmonary disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atypical sinopulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

krabbe disease, atypical Gene Set

From OMIM Gene-Disease Associations

genes associated with the krabbe disease, atypical phenotype from the curated OMIM Gene-Disease Associations dataset.

gaucher disease, atypical Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaucher disease, atypical phenotype from the curated OMIM Gene-Disease Associations dataset.

Atypical Parkinson Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Parkinson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Krabbe Disease, Atypical, Due To Saposin A Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Krabbe Disease, Atypical, Due To Saposin A Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Gaucher disease Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.

hyaline inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

fibrillary inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

skein-like inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

glial cytoplasmic inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 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.

inclusion conjunctivitis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

inclusion Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term inclusion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

muscle fiber inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle fiber inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neutrophil inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the neutrophil inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle fiber cytoplasmatic inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle fiber cytoplasmatic inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

foam cells with lamellar inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the foam cells with lamellar inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

Epithelial Inclusion Cyst Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Epithelial Inclusion Cyst 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.

Germinal Inclusion Cyst Of Ovary Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Germinal Inclusion Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Muscle Fiber Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Muscle Fiber Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Muscle Fiber Cytoplasmatic Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Muscle Fiber Cytoplasmatic Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ubiquitin-Positive Cerebral Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ubiquitin-Positive Cerebral Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Leukocyte Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Leukocyte Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Neutrophil Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neutrophil Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Foam Cells With Lamellar Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Foam Cells With Lamellar Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

glial cytoplasmic inclusion Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2023 dataset.

nervous system inclusion bodies Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the nervous system inclusion bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

glial cytoplasmic inclusion Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2025 dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Familial encephalopathy with neuroserpin inclusion bodies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Inclusion conjunctivitis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Familial encephalopathy with neuroserpin inclusion bodies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Glial cytoplasmic inclusion Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Glial cytoplasmic inclusion cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Glial cytoplasmic inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

skein-like inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Hyaline inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Fibrillary inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Neutrophil inclusion bodies Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neutrophil inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

coronary artery disease; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis; crohn disease; crohn's disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; graft vs host disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Cystinosis, atypical nephropathic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cystinosis, atypical nephropathic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical hemolytic-uremic syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical hemolytic-uremic syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency, atypical Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency, atypical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disseminated atypical mycobacterial infection Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disseminated atypical mycobacterial infection phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

atypical hemolytic-uremic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the atypical hemolytic-uremic syndrome 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.

Atypical Hemolytic Uremic Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Hemolytic Uremic Syndrome from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, atypical vitelliform Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.

Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 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.

Progressive supranuclear palsy atypical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.

atypical autism Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical autism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical neurofibroma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical neurofibroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical teratoid rhabdoid tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical teratoid rhabdoid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical lipomatous tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical lipomatous tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical choroid plexus papilloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical choroid plexus papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical follicular adenoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical follicular adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical polypoid adenomyoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical polypoid adenomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atypical depressive disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atypical depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical 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.

lung diseases; mycobacterium infections, atypical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; mycobacterium infections, atypical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atypical hemolytic uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atypical hemolytic uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mycobacterium infections, atypical; skin ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mycobacterium infections, atypical; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atypical Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term atypical in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Psychosis (atypical) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Psychosis (atypical) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

atypical scarring of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the atypical scarring of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

atypical scarring of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical scarring of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atypical or prolonged hepatitis Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical or prolonged hepatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atypical nevi (>5mm with irregular edge and pigmentation) Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical nevi (>5mm with irregular edge and pigmentation) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atypical nevi in non-sun exposed areas Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical nevi in non-sun exposed areas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mycobacterium Infections, Atypical Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mycobacterium Infections, Atypical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Atypical dual specificity phosphatase, subfamily B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Atypical dual specificity phosphatase, subfamily B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Atypical dual specificity phosphatase, subfamily A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Atypical dual specificity phosphatase, subfamily A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Atypical dual specificity phosphatase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Atypical dual specificity phosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive atypical Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonia congenita, atypical, acetazolamide-responsive Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotonia congenita, atypical, acetazolamide-responsive phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

cystinosis, atypical nephropathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystinosis, atypical nephropathic phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

Atypical NF-kappaB pathway Gene Set

From PID Pathways

proteins participating in the Atypical NF-kappaB pathway pathway from the PID Pathways dataset.

Atypical Teratoid Rhabdoid Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Teratoid Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET 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.

Atypical Ductal Breast Hyperplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Ductal Breast Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Lipoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Lipoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Fibroxanthoma Of Skin Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Fibroxanthoma Of Skin 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.

Atypical Hemolytic Uremic Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adult Atypical Meningioma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Adult Atypical Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Meningioma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Carcinoid Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Carcinoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Spitz Nevus Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Spitz Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Small Acinar Proliferation Of The Prostate Gland Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Small Acinar Proliferation Of The Prostate Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Lobular Breast Hyperplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Lobular Breast Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Endometrial Hyperplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Endometrial Hyperplasia 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.

Atypical Parkinsonism Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Endometriosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Endometriosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Complex Atypical Endometrial Hyperplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Complex Atypical Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Autism Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Autism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Juvenile Parkinsonism Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Juvenile Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Or Prolonged Hepatitis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Or Prolonged Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Pulmonary Carcinoid Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Pulmonary Carcinoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intermediate Atypical Prostate Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intermediate Atypical Prostate Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Lymphoproliferative Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Lymphoproliferative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Burkitt'S Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Burkitt'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Werner Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Werner Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Childhood Atypical Teratoid/Rhabdoid Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Childhood Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Medullary Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Medullary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Hypotonia Cystinuria Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Hypotonia Cystinuria Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Follicular Adenoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Follicular Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Polypoid Adenomyoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Polypoid Adenomyoma 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.

Atypical Adenoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Recurrent Atypical Teratoid/Rhabdoid Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Recurrent Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Neurofibroma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Neurofibroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Cystic Fibrosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Absence Seizure Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Absence Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Depressive Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cystinosis, Atypical Nephropathic (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cystinosis, Atypical Nephropathic (Disorder) 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.

Atypical Benign Partial Epilepsy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Benign Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Psychosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Psychosis 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.

Incontinentia Pigmenti, Atypical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Incontinentia Pigmenti, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Angina Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Angina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hutchinson-Gilford Progeria Syndrome, Atypical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hutchinson-Gilford Progeria Syndrome, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive, 1, Atypical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Supranuclear Palsy, Progressive, 1, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Pneumonia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Primary Atypical Pneumonia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Primary Atypical Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Aniridia, Atypical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Aniridia, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Scrapie Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Scrapie in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Myotonia Congenita, Atypical, Acetazolamide-Responsive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Myotonia Congenita, Atypical, Acetazolamide-Responsive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Teratoid Tumor, Atypical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Teratoid Tumor, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Subacute Thyroiditis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Subacute Thyroiditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Choroid Plexus Papilloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Choroid Plexus Papilloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Adenomatous Lung Hyperplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atypical Adenomatous Lung Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atypical Scarring Of Skin Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Scarring Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Lymphocyte Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Lymphocyte in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Nevi In Non-Sun Exposed Areas Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Nevi In Non-Sun Exposed Areas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Femoral Fracture Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Femoral Fracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Chest Pain Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Chest Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Hyperphenylalaninemia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Hyperphenylalaninemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical memory B cell_Venous blood_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Atypical memory B cell_Venous blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Atypical memory B cell_Peripheral blood_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Atypical memory B cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Atypical B cell(ABC)_Peripheral blood_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Atypical B cell(ABC)_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Atypical hemolytic-uremic syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Atypical hemolytic-uremic syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Atypical teratoid rhabdoid tumor Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Atypical teratoid rhabdoid tumor from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Atypical depressive disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical hemolytic-uremic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical hemolytic-uremic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical autism Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical autism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical teratoid rhabdoid tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical teratoid rhabdoid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical chronic myeloid leukemia, BCR-ABL1 negative Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical chronic myeloid leukemia, BCR-ABL1 negative in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical polypoid adenomyoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical polypoid adenomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical choroid plexus papilloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical choroid plexus papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical neurofibroma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical neurofibroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical follicular adenoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical follicular adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical dopamine transporter deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atypical dopamine transporter deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atypical ductal hyperplasia cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Atypical ductal hyperplasia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Atypical hemolytic-uremic syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical hemolytic-uremic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical Rett syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical Rett syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical teratoid rhabdoid tumor Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical teratoid rhabdoid tumor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical behavior Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical behavior phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical endometrial hyperplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical endometrial hyperplasia 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.

Disseminated atypical mycobacterial infection Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Disseminated atypical mycobacterial infection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical coarctation of aorta Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical coarctation of aorta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical cerebral palsy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical cerebral palsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical glycine encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical glycine encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atypical chronic myeloid leukemia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atypical chronic myeloid leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Psychosis (atypical) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Psychosis (atypical) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Bisphosphonate-associated atypical femoral fracture Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Bisphosphonate-associated atypical femoral fracture phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Atypical femoral fracture in phosphonate treatment Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Atypical femoral fracture in phosphonate treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

crohn disease; crohn's disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma 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.

coronary disease; coronary heart disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

liver disease; wilson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; dna damage; genomic instability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease ; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; sarcoidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; sarcoidosis 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.

addison's disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult-onset still disease; still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amnesia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; nervous system diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; metabolic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft-versus-host disease; psoriasis; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; gastrointestinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease; ulcerative colitis; inflammatory bowel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; periodontal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; ileal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

common variable immunodeficiency; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dilatation, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sanhoff disease; tay-sachs disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease/coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hallucinations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction 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.

ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroid disease; thyroid disease, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylarthropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Crohn's disease and celiac disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiovascular Disease+Pulmonary Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Parkinson's disease or first degree relation to individual with Parkinson's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Alzheimer's disease or family history of Alzheimer's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Crohn's disease and celiac disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors Gene Set

From Biocarta Pathways

proteins participating in the inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors pathway from the Biocarta Pathways dataset.

deregulation of cdk5 in alzheimers disease Gene Set

From Biocarta Pathways

proteins participating in the deregulation of cdk5 in alzheimers disease pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

Parkinson disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature coronary artery disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jakob-Creutzfeldt disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jakob-Creutzfeldt disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher's disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stargardt Disease 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stargardt Disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Norum disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Salla disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Worth disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ménière's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ménière's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acute neuronopathic Gaucher's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IVF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type IXa1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive hypophosphatemic bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory bowel disease 25, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Moyamoya disease 6 with achalasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Moyamoya disease 6 with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IV, congenital neuromuscular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B3 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.

Charcot-Marie-Tooth disease, type 4B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain small vessel disease with hemorrhage Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

RRM2B-related mitochondrial disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phytanic acid storage disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 20, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasemia with bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chylomicron retention disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coronary artery disease, autosomal dominant 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hepatic venoocclusive disease with immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Triglyceride storage disease with ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type II, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-pick disease, intermediate, protracted neurovisceral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-pick disease, intermediate, protracted neurovisceral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, autosomal recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudo von Willebrand disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, juvenile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Darier disease, segmental Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, segmental phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Naxos disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Naxos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leiner disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dowling-degos disease 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dowling-degos disease 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor II deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease 0, muscle Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Subacute neuronopathic Gaucher's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lafora disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lafora disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type X Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tangier disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tangier disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cole disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cole disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 8, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXa2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Refsum disease, adult, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Werdnig-Hoffmann disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 19, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cholestanol storage disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-sachs disease, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stargardt disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor IX deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alexander's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal arthrogryposis with anterior horn cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dowling-Degos disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dowling-Degos disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, B1 variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mast cell disease, systemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mast cell disease, systemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutral lipid storage disease with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor XI deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease XV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemoglobin H disease, nondeletional Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemoglobin H disease, nondeletional phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXb Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle eye brain disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Addison's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Addison's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital cystic disease of liver Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lhermitte-Duclos disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kugelberg-Welander disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kugelberg-Welander disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Darier disease, acral hemorrhagic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate d Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate c Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIb Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease ganglioneuroblastoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oguchi's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kanzaki disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic valve disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intermediate maple syrup urine disease type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intermediate maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fish-eye disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, chronic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Central core disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor VIII deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, variant AB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sialic acid storage disease, severe infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

I cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the I cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, multisystem, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Medullary cystic kidney disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Danon disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dent disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXd Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, syndromic multisystem Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, syndromic multisystem phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset.

Pick Disease of the Brain Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 10 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 12 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 13 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 14 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 15 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 18 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 18 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 19 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 19 from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.

Parkinson disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset.

Oguchi disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease from the curated CTD Gene-Disease Associations dataset.

Tay-Sachs Disease, AB Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset.

Naxos disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Naxos disease from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset.

Carbamoyl-Phosphate Synthase I Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Chylomicron retention disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset.

Cholesterol Ester Storage Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 6 from the curated CTD Gene-Disease Associations dataset.

Addison Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset.

Alexander Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 16 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 17 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 7 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 4 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease 0, Liver Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset.

Tangier Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tangier Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 26 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 26 from the curated CTD Gene-Disease Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.

Hartnup Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset.

Intervertebral disc disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intervertebral disc disease from the curated CTD Gene-Disease Associations dataset.

Von Willebrand disease, platelet type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset.

Coronary Artery Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease from the curated CTD Gene-Disease Associations dataset.

Machado-Joseph Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease from the curated CTD Gene-Disease Associations dataset.

Papillon-Lefevre Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Papillon-Lefevre Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Moyamoya Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya Disease from the curated CTD Gene-Disease Associations dataset.

Gilbert Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gilbert Disease from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

Pulmonary Disease, Chronic Obstructive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 14 from the curated CTD Gene-Disease Associations dataset.

Coronary Artery Disease, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 9 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 11 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 16 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 12 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 10 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease 0, Muscle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease 0, Muscle from the curated CTD Gene-Disease Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Basal ganglia disease, biotin-responsive from the curated CTD Gene-Disease Associations dataset.

Non-alcoholic Fatty Liver Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Non-alcoholic Fatty Liver Disease from the curated CTD Gene-Disease Associations dataset.

Graves Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Graves Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.

Hepatic Veno-Occlusive Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.

Hepatic venoocclusive disease with immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 25, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 25, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 3 from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 4 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type IV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type IV from the curated CTD Gene-Disease Associations dataset.

Refsum Disease, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.

Polycystic liver disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic liver disease from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Celiac Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Celiac Disease from the curated CTD Gene-Disease Associations dataset.

Genetic Predisposition to Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Genetic Predisposition to Disease from the curated CTD Gene-Disease Associations dataset.

Dimauro disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dimauro disease from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IXB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IXB from the curated CTD Gene-Disease Associations dataset.

Coronary Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease, Secondary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease, Secondary from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4j Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

GALLBLADDER DISEASE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GALLBLADDER DISEASE 1 from the curated CTD Gene-Disease Associations dataset.

Acute Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acute Disease from the curated CTD Gene-Disease Associations dataset.

Brain Small Vessel Disease with Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.

Ornithine Carbamoyltransferase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease, Type IXD Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

GLYCOGEN STORAGE DISEASE IXa1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE IXa1 from the curated CTD Gene-Disease Associations dataset.

Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease XII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease XII from the curated CTD Gene-Disease Associations dataset.

Legionnaires' Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Legionnaires' Disease from the curated CTD Gene-Disease Associations dataset.

Hepatorenal form of glycogen storage disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.

Schindler Disease, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schindler Disease, Type I from the curated CTD Gene-Disease Associations dataset.

Pulmonary Veno-Occlusive Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 3 from the curated CTD Gene-Disease Associations dataset.

Refsum Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Refsum Disease from the curated CTD Gene-Disease Associations dataset.

Aland Island Eye Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset.

Bowen's Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bowen's Disease from the curated CTD Gene-Disease Associations dataset.

Hodgkin Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin Disease from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 2 from the curated CTD Gene-Disease Associations dataset.

Pyruvate Dehydrogenase Complex Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 13 from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.

Medullary Cystic Kidney Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset.

von Willebrand Disease, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease von Willebrand Disease, Type 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset.

Huntington Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease from the curated CTD Gene-Disease Associations dataset.

PAGET DISEASE, JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PAGET DISEASE, JUVENILE from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE, LATE-ONSET Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset.

Neutral Lipid Storage Disease with Myopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset.

End Stage Liver Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease End Stage Liver Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 5 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 6 from the curated CTD Gene-Disease Associations dataset.

Hashimoto Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hashimoto Disease from the curated CTD Gene-Disease Associations dataset.

Canavan Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Canavan Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 1 from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease XIII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset.

Lafora Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lafora Disease from the curated CTD Gene-Disease Associations dataset.

Van Buchem disease type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Van Buchem disease type 2 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Disease Models, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Models, Animal from the curated CTD Gene-Disease Associations dataset.

Fabry Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fabry Disease from the curated CTD Gene-Disease Associations dataset.

Motor Neuron Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type A from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type VII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type VII from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 3 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 5 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 8 from the curated CTD Gene-Disease Associations dataset.

dowling-degos disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Darier Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Darier Disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease from the curated CTD Gene-Disease Associations dataset.

Paget Disease Of Bone 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset.

Disease Progression Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Progression from the curated CTD Gene-Disease Associations dataset.

Disease Susceptibility Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Susceptibility from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset.

Dent Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dent Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 16 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 12 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

De Vivo disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease De Vivo disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer disease type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer disease type 4 from the curated CTD Gene-Disease Associations dataset.

Alzheimer disease type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer disease type 2 from the curated CTD Gene-Disease Associations dataset.

Leigh Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leigh Disease from the curated CTD Gene-Disease Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 28, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 28, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B 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.

Glycogen Storage Disease IXC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IXC from the curated CTD Gene-Disease Associations dataset.

Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.

AORTIC VALVE DISEASE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type VI Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IB from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 10 from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type B from the curated CTD Gene-Disease Associations dataset.

Raynaud Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Raynaud Disease from the curated CTD Gene-Disease Associations dataset.

Moyamoya disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya disease 1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type IIb Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type IIb from the curated CTD Gene-Disease Associations dataset.

Moyamoya disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya disease 3 from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick disease, type C2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick disease, type C2 from the curated CTD Gene-Disease Associations dataset.

Hodgkin disease, X-linked pseudoautosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 8 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 9 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 7 from the curated CTD Gene-Disease Associations dataset.

Sialic Acid Storage Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sialic Acid Storage Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 24 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 24 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset.

Gallbladder Disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gallbladder Disease 4 from the curated CTD Gene-Disease Associations dataset.

Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 20 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 22 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 22 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 27 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 27 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 21 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 15 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 23 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.

GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Peripheral Arterial Occlusive Disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Arterial Occlusive Disease 1 from the curated CTD Gene-Disease Associations dataset.

Maple Syrup Urine Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maple Syrup Urine Disease from the curated CTD Gene-Disease Associations dataset.

GLYCOGEN STORAGE DISEASE XV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE XV from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Type Iiic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Type Iiic from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B2 from the curated CTD Gene-Disease Associations dataset.

von Hippel-Lindau Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease von Hippel-Lindau Disease from the curated CTD Gene-Disease Associations dataset.

Multiple Sulfatase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset.

Graft vs Host Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Graft vs Host Disease from the curated CTD Gene-Disease Associations dataset.

Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4B1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B1 from the curated CTD Gene-Disease Associations dataset.

Pelizaeus-Merzbacher Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pelizaeus-Merzbacher Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type I from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

Sandhoff Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sandhoff Disease from the curated CTD Gene-Disease Associations dataset.

von Willebrand Disease, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease von Willebrand Disease, Type 2 from the curated CTD Gene-Disease Associations dataset.

von Willebrand Disease, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease von Willebrand Disease, Type 1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IC from the curated CTD Gene-Disease Associations dataset.

Coronary Artery Disease, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Desmoid disease, hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Desmoid disease, hereditary from the curated CTD Gene-Disease Associations dataset.

Pyruvate Carboxylase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Carboxylase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Perinatal Lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Perinatal Lethal from the curated CTD Gene-Disease Associations dataset.

Gestational Trophoblastic Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gestational Trophoblastic Disease from the curated CTD Gene-Disease Associations dataset.

Crohn Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Crohn Disease from the curated CTD Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 11, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 11, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Gerstmann-Straussler-Scheinker Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gerstmann-Straussler-Scheinker Disease from the curated CTD Gene-Disease Associations dataset.

Dent disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dent disease 1 from the curated CTD Gene-Disease Associations dataset.

Norrie disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Norrie disease from the curated CTD Gene-Disease Associations dataset.

Rippling muscle disease, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rippling muscle disease, 1 from the curated CTD Gene-Disease Associations dataset.

Tay-Sachs Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tay-Sachs Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4B2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B2 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type V Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type V from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Legg-Calve-Perthes Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Legg-Calve-Perthes Disease from the curated CTD Gene-Disease Associations dataset.

Medullary cystic kidney disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Medullary cystic kidney disease 1 from the curated CTD Gene-Disease Associations dataset.

Celiac Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Celiac Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Coronary Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Coronary Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Hirschsprung Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hirschsprung Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Gaucher Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Gaucher Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Alzheimer Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Alzheimer Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Non-alcoholic Fatty Liver Disease [Supplementary Concept] Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Non-alcoholic Fatty Liver Disease [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Hodgkin Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hodgkin Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Coronary Artery Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Coronary Artery Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Paget's disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Paget's disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Parkinson Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Parkinson Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Moyamoya Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Moyamoya Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Pulmonary Disease, Chronic Obstructive Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Crohn Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Crohn Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Nonalcoholic Fatty Liver Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Nonalcoholic Fatty Liver Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Graves Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Graves Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

autoimmune disease of gastrointestinal tract Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease autoimmune disease of gastrointestinal tract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bronchial disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease bronchial disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

collagen disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease collagen disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

diaphragm disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease diaphragm disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

impaired renal function disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease impaired renal function disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone remodeling disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

polycystic kidney disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease polycystic kidney disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone marrow disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease bone marrow disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

lafora disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease lafora disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autosomal recessive disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease autosomal recessive disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

systemic primary carnitine deficiency disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease systemic primary carnitine deficiency disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

danon disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease danon disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

pigmentation disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease pigmentation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autosomal dominant disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease autosomal dominant disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

integumentary system disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease integumentary system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

gaucher's disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease gaucher's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

thomsen disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease thomsen disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

demyelinating disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease demyelinating disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

celiac disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease celiac disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood platelet disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease blood platelet disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

caffey disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease caffey disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

iris disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease iris disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

cerebellar disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease cerebellar disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

eye disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease eye disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sex differentiation disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease sex differentiation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

basal ganglia disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease basal ganglia disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ocular motility disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease ocular motility disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

pancreas disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease pancreas disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

kennedy's disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease kennedy's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autosomal genetic disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease autosomal genetic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

acquired metabolic disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease acquired metabolic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

wolman disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease wolman disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of endocrine system Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease autoimmune disease of endocrine system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone development disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease bone development disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

chronic myeloproliferative disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease chronic myeloproliferative disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

uveal disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease uveal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart valve disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease heart valve disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fabry disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease fabry disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

teeth hard tissue disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease teeth hard tissue disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

glycogen storage disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease glycogen storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital heart disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart conduction disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease heart conduction disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

lens disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease lens disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

adnexa disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

krabbe disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease krabbe disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood protein disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease blood protein disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

lymph node disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease lymph node disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

hair disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease hair disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sinoatrial node disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease sinoatrial node disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

refsum disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease refsum disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

arteriosclerotic cardiovascular disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease arteriosclerotic cardiovascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease x-linked disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

biliary tract disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease biliary tract disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ovarian disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease ovarian disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

gastrointestinal system disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease gastrointestinal system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

obstructive lung disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease obstructive lung disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

myotonic disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease myotonic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

glycogen storage disease vii Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease glycogen storage disease vii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

carbohydrate metabolism disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease carbohydrate metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

norum disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease norum disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

female reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease female reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

skin disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease skin disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

chromosomal disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease chromosomal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

central nervous system disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease central nervous system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

adrenal cortex disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease adrenal cortex disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

monogenic disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease monogenic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

atrophic muscular disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease atrophic muscular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

tooth disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease tooth disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral vascular disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease peripheral vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

cholesterol ester storage disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease cholesterol ester storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

liver disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease liver disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mitochondrial metabolism disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease mitochondrial metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

alzheimer's disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease alzheimer's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

lung disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease lung disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sweat gland disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease sweat gland disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

plasma protein metabolism disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease plasma protein metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

tangier disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease tangier disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

paget's disease of bone Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease paget's disease of bone from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

testicular disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease testicular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bartter disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease bartter disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

inflammatory bowel disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease inflammatory bowel disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.