Upper airway obstruction

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Results for "Upper airway obstruction": 1 gene, 393 gene sets

Name
UCMA Gene upper zone of growth plate and cartilage matrix associated This gene encodes a chondrocyte-specific, highly charged protein that is abundantly expressed in the upper immature zone of fetal and juvenile epiphyseal cartilage. The encoded protein undergoes proteolytic processing to generate a mature protein that is secreted into the extracellular matrix. The glutamic acid residues in the encoded protein undergo gamma carboxylation in a vitamin K-dependent manner. Undercarboxylation of the encoded protein is associated with osteoarthritis in humans. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2015]
upper airway obstruction Gene Set From HPO Gene-Disease Associations genes associated with the upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Upper Airway Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
episodic upper airway obstruction Gene Set From HPO Gene-Disease Associations genes associated with the episodic upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Episodic Upper Airway Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Airway Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Airway Obstruction from the curated CTD Gene-Disease Associations dataset.
airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
airway obstruction; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease airway obstruction; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Airway Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Airway Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lower Airway Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lower Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Airway obstruction (FEV1/FVC<70%) in never smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway obstruction (FEV1/FVC<70%) in never smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airway obstruction (FEV1/FVC Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway obstruction (FEV1/FVC
Upper Airway Resistance Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Resistance Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
airway remodeling; nasal polyps; recurrence; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease airway remodeling; nasal polyps; recurrence; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
airway hyperresponsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease airway hyperresponsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased airway responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased airway responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
airway remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease airway remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory airway resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory airway resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
airway Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term airway in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Airway hyperresponsiveness Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Airway hyperresponsiveness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
chronic rhinitis due to narrow nasal airway Gene Set From HPO Gene-Disease Associations genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Airway Remodeling Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Airway Remodeling phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal airway responsiveness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal airway responsiveness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased airway responsiveness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased airway responsiveness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased airway responsiveness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased airway responsiveness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal airway basal cell differentiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal airway basal cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal airway basal cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal airway basal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
airway basal cell hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the airway basal cell hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
airway fluid Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue airway fluid in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Chronic Obstructive Airway Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Obstructive Airway Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Airway Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Airway Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reactive Airway Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reactive Airway Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Rhinitis Due To Narrow Nasal Airway Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Rhinitis Due To Narrow Nasal Airway in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Airway Disease Restrictive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Airway Disease Restrictive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Airway Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Airway Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Airway Remodeling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Airway Remodeling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
increased airway responsiveness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased airway responsiveness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased airway responsiveness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased airway responsiveness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal airway responsiveness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal airway responsiveness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal airway basal cell differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal airway basal cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
airway basal cell hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the airway basal cell hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased airway resistance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased airway resistance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
decreased airway resistance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased airway resistance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Human - Lung v1 - L2 - Airway Smooth Muscle Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Airway Smooth Muscle cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Lung v2 (HLCA) - L2 - Airway epithelium Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L2 - Airway epithelium cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Airway dendritic cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Airway dendritic cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Airway secretory cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Airway secretory cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Airway smooth muscle cell_Bronchial vessel_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Airway smooth muscle cell_Bronchial vessel_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Ciliated airway epithelial cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Ciliated airway epithelial cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Airway cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Airway cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Airway basal cell_Trachea_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Airway basal cell_Trachea_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Airway smooth muscle cell contraction Gene Set From WikiPathways Pathways 2024 proteins participating in the Airway smooth muscle cell contraction pathway from the WikiPathways Pathways 2024 dataset.
Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron cell type from the HuBMAP ASCT+B dataset.
Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Airway fluid Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Airway fluid in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Congenital Pulmonary Airway Malformations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital Pulmonary Airway Malformations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Airway imaging phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway imaging phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airway responsiveness in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway responsiveness in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airway wall thickness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway wall thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airway hyperresponsiveness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway hyperresponsiveness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nasal Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nasal Obstruction from the curated CTD Gene-Disease Associations dataset.
Renal Artery Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Artery Obstruction from the curated CTD Gene-Disease Associations dataset.
Intestinal Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intestinal Obstruction from the curated CTD Gene-Disease Associations dataset.
Ventricular Outflow Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Outflow Obstruction from the curated CTD Gene-Disease Associations dataset.
Urinary Bladder Neck Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Urinary Bladder Neck Obstruction from the curated CTD Gene-Disease Associations dataset.
Ureteral Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ureteral Obstruction from the curated CTD Gene-Disease Associations dataset.
intestinal pseudo-obstruction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
intestinal obstruction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intestinal obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
gastric outlet obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric outlet obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary tract obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lacrimal duct obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
colonic pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ureteral obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureteral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bladder neck obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bladder neck obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urethral obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urethral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal artery obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal artery obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duodenal obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duodenal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atherosclerosis; hypertension, renovascular; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension, renovascular; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intestinal pseudo-obstruction; mitochondrial diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hypertension; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late-onset airflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease late-onset airflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; intestinal obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; intestinal obstruction 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.
deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction 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.
obstruction Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term obstruction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Airflow obstruction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Airflow obstruction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
gastric outlet obstruction Gene Set From GWASdb SNP-Disease Associations genes associated with the disease gastric outlet obstruction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
urethral obstruction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the urethral obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
gastrointestinal obstruction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the gastrointestinal obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
intestinal obstruction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the intestinal obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
intestinal obstruction Gene Set From HPO Gene-Disease Associations genes associated with the intestinal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intestinal pseudo-obstruction Gene Set From HPO Gene-Disease Associations genes associated with the intestinal pseudo-obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gastrointestinal obstruction Gene Set From HPO Gene-Disease Associations genes associated with the gastrointestinal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right ventricular outlet obstruction Gene Set From HPO Gene-Disease Associations genes associated with the right ventricular outlet obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nasal obstruction Gene Set From HPO Gene-Disease Associations genes associated with the nasal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nasolacrimal duct obstruction Gene Set From HPO Gene-Disease Associations genes associated with the nasolacrimal duct obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ureteropelvic junction obstruction Gene Set From HPO Gene-Disease Associations genes associated with the ureteropelvic junction obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ureteral obstruction Gene Set From HPO Gene-Disease Associations genes associated with the ureteral obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
urethral obstruction Gene Set From HPO Gene-Disease Associations genes associated with the urethral obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Nasal Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Nasal Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Artery Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Artery Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Intestinal Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intestinal Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Outflow Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Outflow Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Gastric Outlet Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gastric Outlet Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Intestinal Pseudo-Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intestinal Pseudo-Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ureteral Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ureteral Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
urinary bladder obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the urinary bladder obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureterovesical junction obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureterovesical junction obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intestinal obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
rete testis obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the rete testis obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureteropelvic junction obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureteropelvic junction obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureter obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureter obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
urethra obstruction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the urethra obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pelviureteric junction obstruction Gene Set From OMIM Gene-Disease Associations genes associated with the pelviureteric junction obstruction phenotype from the curated OMIM Gene-Disease Associations dataset.
Obstruction Of Biliary Tree Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstruction Of Biliary Tree in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urinary Tract Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Intestinal Pseudo-Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Pseudo-Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bladder Neck Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bladder Neck Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ureterovesical Junction Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ureterovesical Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prostatic Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urinary Outflow Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urinary Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Nasal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Nasal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Ureteropelvic Junction Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Ureteropelvic Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Obstruction Of Bladder Neck Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Obstruction Of Bladder Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urethral Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urethral Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bronchial Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bronchial Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Airflow Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Airflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Outflow Tract Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Outflow Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Ileal Obstruction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Ileal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Intestinal Obstruction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urethral Obstruction Sequence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urethral Obstruction Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstruction Of Colon Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstruction Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Urinary Tract Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duodenal Obstruction Due To Malrotation Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duodenal Obstruction Due To Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Portal Vein Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Portal Vein Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Biliary Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Biliary Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lacrimal Duct Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ventricular Outflow Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bladder Outflow Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bladder Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Bowel Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Bowel Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Nasal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Nasal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Acquired Nasolacrimal Duct Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Artery Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Artery Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Pelviureteric Junction Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Pelviureteric Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Ureteric Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Ureteric Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ureteral Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ureteral Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nasal Obstruction Present Finding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nasal Obstruction Present Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Functional Intestinal Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Laryngeal Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Laryngeal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Malignant Bowel Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Bowel Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Obstruction Of Nasolacrimal Duct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Obstruction Of Nasolacrimal Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Obstruction Of Pelviureteric Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Obstruction Of Pelviureteric Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Outflow Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stricture Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stricture Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gastrointestinal Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lymphatic Obstruction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lymphatic Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
intestinal obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ureteropelvic junction obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ureteropelvic junction obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ureterovesical junction obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ureterovesical junction obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
rete testis obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the rete testis obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
urinary bladder obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the urinary bladder obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
urethra obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the urethra obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ureter obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ureter obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nasal obstruction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nasal obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
urinary bladder obstruction Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the urinary bladder obstruction phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Intestinal pseudo-obstruction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Intestinal obstruction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Intestinal obstruction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastric outlet obstruction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Gastric outlet obstruction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ureteropelvic junction obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ureteropelvic junction obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urinary tract obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ureteral obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ureteral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duodenal obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duodenal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastric outlet obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastric outlet obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Colonic pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urethral obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urethral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lacrimal duct obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bladder neck obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bladder neck obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal artery obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal artery obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal pseudo-obstruction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal pseudo-obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intestinal obstruction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lower urinary tract obstruction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower urinary tract obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial congenital nasolacrimal duct obstruction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial congenital nasolacrimal duct obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Airflow obstruction in ever smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airflow obstruction in ever smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airflow obstruction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airflow obstruction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Primary somatosensory area, upper limb, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper dorsal perifornical nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper dorsal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper dorsal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper dorsal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper basal perifornical nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper basal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, upper limb, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper basal lateral hypothalamic area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
upper (rostral) rhombic lip_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
upper (rostral) rhombic lip_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
upper (rostral) rhombic lip_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
upper (rostral) rhombic lip_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
upper limb region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in upper limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
external granular (germinal) layer of upper rhombic lip Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in external granular (germinal) layer of upper rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
upper (rostral) rhombic lip Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in upper (rostral) rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Single upper central incisor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Single upper central incisor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Single upper central incisor from the curated CTD Gene-Disease Associations dataset.
upper respiratory tract disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
upper respiratory tract disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mononeuritis of upper limb and mononeuritis multiplex Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
H3K4me3_fibroblast of upper leg skin_hg19_1 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
H3K4me3_fibroblast of upper leg skin_hg19_2 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
CTCF_fibroblast of upper leg skin_hg19_2 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
CTCF_fibroblast of upper leg skin_hg19_1 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
adenocarcinoma of the upper gastrointestinal tract. Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma of the upper gastrointestinal tract. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tumours of the upper aerodigestive tract Gene Set From GAD Gene-Disease Associations genes associated with the disease tumours of the upper aerodigestive tract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
upper aerodigestive tract cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
upper aerodigestive tract cancers Gene Set From GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
upper Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term upper in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Bone mineral density (paediatric, upper limb) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Upper aerodigestive tract cancers Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Upper aerodigestive tract cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
upper respiratory tract disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease upper respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of upper limb bone Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
diaphyseal sclerosis of the upper limbs Gene Set From GWASdb SNP-Phenotype Associations genes associated with the diaphyseal sclerosis of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the upper urinary tract Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the upper limb Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of upper limb metaphysis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sclerosis of metaphyses of the upper limbs Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sclerosis of metaphyses of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the upper arm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
anomaly of the upper limb diaphyses Gene Set From GWASdb SNP-Phenotype Associations genes associated with the anomaly of the upper limb diaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of upper lip Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased upper to lower segment ratio Gene Set From HPO Gene-Disease Associations genes associated with the increased upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal upper limb muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper arm Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper limb bone Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
u-shaped upper lip vermilion Gene Set From HPO Gene-Disease Associations genes associated with the u-shaped upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb metaphyseal widening Gene Set From HPO Gene-Disease Associations genes associated with the upper limb metaphyseal widening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the musculature of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tented upper lip vermilion Gene Set From HPO Gene-Disease Associations genes associated with the tented upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the upper limb Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper limb epiphysis morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the upper arm Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft upper lip Gene Set From HPO Gene-Disease Associations genes associated with the cleft upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal upper motor neuron morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper limb metaphysis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
everted upper lip vermilion Gene Set From HPO Gene-Disease Associations genes associated with the everted upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper eyelid coloboma Gene Set From HPO Gene-Disease Associations genes associated with the upper eyelid coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hyporeflexia of upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the hyporeflexia of upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper limb joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of bones involving the upper extremities Gene Set From HPO Gene-Disease Associations genes associated with the duplication of bones involving the upper extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the musculature of the upper arm Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short upper lip Gene Set From HPO Gene-Disease Associations genes associated with the short upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
synostosis involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the synostosis involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb postural tremor Gene Set From HPO Gene-Disease Associations genes associated with the upper limb postural tremor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal upper limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal morphology of bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb phocomelia Gene Set From HPO Gene-Disease Associations genes associated with the upper limb phocomelia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent upper and lower respiratory tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long upper lip Gene Set From HPO Gene-Disease Associations genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb spasticity Gene Set From HPO Gene-Disease Associations genes associated with the upper limb spasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal upper limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal upper to lower segment ratio Gene Set From HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thick upper lip vermilion Gene Set From HPO Gene-Disease Associations genes associated with the thick upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the upper respiratory tract Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the upper respiratory tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
flared upper limb metaphysis Gene Set From HPO Gene-Disease Associations genes associated with the flared upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper lip vermillion Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper lip vermillion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thin upper lip vermilion Gene Set From HPO Gene-Disease Associations genes associated with the thin upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent upper respiratory tract infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb undergrowth Gene Set From HPO Gene-Disease Associations genes associated with the upper limb undergrowth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal muscle weakness in upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the proximal muscle weakness in upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the upper urinary tract Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the upper urinary tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
contractures of the joints of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the contractures of the joints of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb muscle hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper extremity joint dislocation Gene Set From HPO Gene-Disease Associations genes associated with the upper extremity joint dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Upper Extremity Deformities, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Upper Extremity Deformities, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Upper Extremity Deep Vein Thrombosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Upper Extremity Deep Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
absent upper incisors Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent upper incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal upper lip morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal upper lip morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
upper epidermis Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue upper epidermis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Upper Limb Asymmetry Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Asymmetry in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Upper Respiratory Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Limb Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical Diaphyseal Thickening Of The Upper Limbs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical Diaphyseal Thickening Of The Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Upper Motor Neuron Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Upper Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Limb Peromelia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Peromelia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Upper Limb Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Upper Respiratory Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Upper Respiratory Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Gastrointestinal Symptoms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Gastrointestinal Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Gi Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Gi Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Extremity Deep Vein Thrombosis, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Extremity Deep Vein Thrombosis, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Upper Lip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phocomelia Of Upper Limb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phocomelia Of Upper Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Upper Lip Vermillion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Upper Lip Vermillion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thick Upper Lip Vermilion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Right Upper Quadrant Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Upper Quadrant Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thin Upper Lip Vermilion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thin Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tented Upper Lip Vermilion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tented Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Spasticity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Hypertonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Hypertonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Upper Limb Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Upper And Lower Respiratory Tract Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyperreflexia In Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperreflexia In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Upper Lip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Postural Tremor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Postural Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Muscle Weakness In Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Everted Upper Lip Vermilion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Everted Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Upper Limb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Upper Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Long Upper Lip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyporeflexia Of Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyporeflexia Of Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
U-Shaped Upper Lip Vermilion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype U-Shaped Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Extremity Paresis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Extremity Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Abdominal Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Midline Notch Of Upper Alveolar Ridge Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midline Notch Of Upper Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Upper Urinary Tract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Upper Urinary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Upper Limb Amyotrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Upper To Lower Segment Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Upper To Lower Segment Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Dysmetria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Dysmetria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Signs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Back Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Muscle Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Upper Limb Muscle Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Subcutaneous Adipose Tissue From Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue From Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Osteolysis Involving Bones Of The Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolysis Involving Bones Of The Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Upper To Lower Segment Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Upper To Lower Segment Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Limb Muscle Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Muscle Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Lip Pit Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Lip Pit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Upper Limb Bone Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Upper Limb Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Upper Limb Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Upper Limb Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
short upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lower jaw to upper jaw transformation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lower jaw to upper jaw transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal upper incisor morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper incisor morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unilateral cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bilateral cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
long upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the long upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal upper lip morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper lip morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal upper incisor color Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper incisor color phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
midline cleft upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the midline cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fused upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fused upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thick upper lip Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thick upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
upper jaw to lower jaw transformation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the upper jaw to lower jaw transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small upper incisors Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Upper neuron_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper neuron_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer cell_Prefrontal cortex_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer cell_Prefrontal cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer cortical neuron_Cortex_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer cortical neuron_Cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 2 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 2 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 3 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 3 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 4 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 4 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper Wound Fibroblast_Skin_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper Wound Fibroblast_Skin_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper respiratory tract disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Upper respiratory tract disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mononeuritis of upper limb and mononeuritis multiplex Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diplegia of upper limb Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diplegia of upper limb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Upper lip cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Upper lip cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Upper epidermis Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Upper epidermis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Upper tip-link density Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Upper tip-link density cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Finnish upper limb-onset distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Facial morphology (factor 17, height of vermillion upper lip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial morphology (factor 17, height of vermillion upper lip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (paediatric, upper limb) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Upper eyelid sagging severity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Upper eyelid sagging severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Upper eyelid morphology Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Upper eyelid morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

UCMA Gene

upper airway obstruction Gene Set

Upper Airway Obstruction Gene Set

episodic upper airway obstruction Gene Set

Episodic Upper Airway Obstruction Gene Set

Airway Obstruction Gene Set

airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set

airway obstruction; asthma Gene Set

Airway Obstruction Gene Set

Lower Airway Obstruction Gene Set

Airway obstruction (FEV1/FVC<70%) in never smokers Gene Set

Airway obstruction (FEV1/FVC Gene Set

Upper Airway Resistance Sleep Apnea Syndrome Gene Set

airway remodeling; nasal polyps; recurrence; sinusitis Gene Set

airway hyperresponsiveness Gene Set

decreased airway responsiveness Gene Set

airway remodeling Gene Set

respiratory airway resistance Gene Set

airway Gene Set

Airway hyperresponsiveness Gene Set

chronic rhinitis due to narrow nasal airway Gene Set

Airway Remodeling Gene Set

abnormal airway responsiveness Gene Set

increased airway responsiveness Gene Set

decreased airway resistance Gene Set

increased airway resistance Gene Set

decreased airway responsiveness Gene Set

abnormal airway basal cell differentiation Gene Set

abnormal airway basal cell morphology Gene Set

airway basal cell hyperplasia Gene Set

abnormal airway resistance Gene Set

airway fluid Gene Set

Chronic Obstructive Airway Disease Gene Set

Airway Disease Gene Set

Reactive Airway Disease Gene Set

Chronic Rhinitis Due To Narrow Nasal Airway Gene Set

Airway Disease Restrictive Gene Set

Airway Constriction Gene Set

Airway Remodeling Gene Set

increased airway responsiveness Gene Set

increased airway resistance Gene Set

decreased airway responsiveness Gene Set

abnormal airway responsiveness Gene Set

decreased airway resistance Gene Set

abnormal airway resistance Gene Set

abnormal airway basal cell differentiation Gene Set

airway basal cell hyperplasia Gene Set

increased airway resistance Gene Set

decreased airway resistance Gene Set

Human - Lung v1 - L2 - Airway Smooth Muscle Gene Set

Human - Lung v2 (HLCA) - L2 - Airway epithelium Gene Set

Airway dendritic cell_Lung_Mouse Gene Set

Airway secretory cell_Lung_Human Gene Set

Airway smooth muscle cell_Bronchial vessel_Human Gene Set

Ciliated airway epithelial cell_Lung_Human Gene Set

Airway cell_Lung_Mouse Gene Set

Airway basal cell_Trachea_Human Gene Set

Airway smooth muscle cell contraction Gene Set

Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene Set

Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene Set

Airway fluid Gene Set

Congenital Pulmonary Airway Malformations Gene Set

Airway imaging phenotypes Gene Set

Airway responsiveness in chronic obstructive pulmonary disease Gene Set

Airway wall thickness Gene Set

Airway hyperresponsiveness Gene Set

Nasal Obstruction Gene Set

Renal Artery Obstruction Gene Set

Intestinal Obstruction Gene Set

Ventricular Outflow Obstruction Gene Set

Urinary Bladder Neck Obstruction Gene Set

Ureteral Obstruction Gene Set

intestinal pseudo-obstruction Gene Set

intestinal obstruction Gene Set

gastric outlet obstruction Gene Set

urinary tract obstruction Gene Set

lacrimal duct obstruction Gene Set

colonic pseudo-obstruction Gene Set

intestinal obstruction Gene Set