Infantile Asthma

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Results for "Infantile Asthma": 13 genes, 646 gene sets

Name
BFIS1 Gene benign familial infantile* convulsions*
NYS5 Gene Nystagmus 5, infantile* periodic alternating*
CLN6 Gene ceroid-lipofuscinosis, neuronal 6, late infantile, variant This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. [provided by RefSeq, Oct 2008]
BFIS4 Gene Convulsions, benign familial infantile, 4
PKDTS Gene polycystic kidney disease, infantile* severe, with tuberous sclerosis*
BFIC2 Gene Benign familial infantile* convulsions-2*
EIM Gene Infantile myoclonic epilepsy
GLC3B Gene glaucoma 3, primary infantile, B
IHPS2 Gene Pyloric stenosis, infantile* hypertrophic, 2*
CMS1A1 Gene myasthenia gravis, familial infantile, 1
IHPS5 Gene Pyloric stenosis, infantile* hypertrophic, 5*
IHPS4 Gene Pyloric stenosis, infantile* hypertrophic, 4*
IHPS3 Gene Pyloric stenosis, infantile* hypertrophic, 3*
Infantile Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
asthma. asthma severity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. asthma severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset.
Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.
Asthma, Aspirin-Induced Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Aspirin-Induced from the curated CTD Gene-Disease Associations dataset.
Asthma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.
Asthma, Exercise-Induced Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Exercise-Induced from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset.
Asthma Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Asthma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
asthma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease asthma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
asthma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease asthma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
intrinsic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intrinsic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cough variant asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cough variant asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
allergic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease allergic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asthma; dermatitis, atopic; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ascariasis; asthma; Gene Set From GAD Gene-Disease Associations genes associated with the disease ascariasis; asthma; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; ige Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; recurrence; respiratory sounds; respiratory syncytial virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; recurrence; respiratory sounds; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; drug hypersensitivity; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; drug hypersensitivity; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; drug hypersensitivity; hypersensitivity, immediate; urticaria Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; drug hypersensitivity; hypersensitivity, immediate; urticaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma and atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma and atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; atopy; dermatitis and eczema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; atopy; dermatitis and eczema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; food hypersensitivity; hypersensitivity, immediate; respiratory sounds; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; food hypersensitivity; hypersensitivity, immediate; respiratory sounds; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eosinophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eosinophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity, immediate; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity, immediate; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; nasal polyps Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; nasal polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; conjunctivitis, allergic; hypersensitivity; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; conjunctivitis, allergic; hypersensitivity; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcerative colitis; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcerative colitis; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease; asthma; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease; asthma; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; rhinitis, allergic Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; rhinitis, allergic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; egg hypersensitivity; food hypersensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; egg hypersensitivity; food hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma, aspirin-induced; urticaria, aspirin-intolerant Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma, aspirin-induced; urticaria, aspirin-intolerant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; eczema; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; eczema; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood only) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; helicobacter infections; hypersensitivity, immediate Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; helicobacter infections; hypersensitivity, immediate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; candidiasis; high-altitude illness Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; candidiasis; high-altitude illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; drug therapy; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; drug therapy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer; asthma; emphysema; bronchitis; pneumonia; hay fever Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer; asthma; emphysema; bronchitis; pneumonia; hay fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (toluene diisocyanate-induced) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (toluene diisocyanate-induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; tuberculosis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. fev(1) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. fev(1) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis and eczema; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis and eczema; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma in men Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma in men in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
drug hypersensitivity; asthma; rhinosinuitis, allergic fungal; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease drug hypersensitivity; asthma; rhinosinuitis, allergic fungal; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atopy. asthma. netherton Gene Set From GAD Gene-Disease Associations genes associated with the disease atopy. asthma. netherton in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; rhinitis, allergic, perennial Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; rhinitis, allergic, perennial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergic rhinitis; atopic dermatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergic rhinitis; atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. total serum ige Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. total serum ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; juvenile arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; drug hypersensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; drug hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; eczema; hypersensitivity, immediate; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; eczema; hypersensitivity, immediate; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; drug hypersensitivity; rhinitis, allergic, perennial; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; drug hypersensitivity; rhinitis, allergic, perennial; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma, exercise-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma, exercise-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atopic asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; respiratory syncytial virus; juvenile arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; respiratory syncytial virus; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; constriction, pathologic; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; constriction, pathologic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood & adult) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood atopic asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
physician diagnosed asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease physician diagnosed asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma smokers Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma smokers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; diseases in twins; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; diseases in twins; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; aspirin intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; aspirin intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma, exercise-induced; bronchial hyperreactivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma, exercise-induced; bronchial hyperreactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; job's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; job's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma or atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma or atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma drug response Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma drug response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; lipids; memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; lipids; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; asthma; lupus erythematosus, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; asthma; lupus erythematosus, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchial hyperreactivity; hypersensitivity, immediate Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchial hyperreactivity; hypersensitivity, immediate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergic rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergic rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; atopy; juvenile arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; atopy; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; endothelium dependent dilatation Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; endothelium dependent dilatation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hiv disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hiv disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchiolitis; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchiolitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; food hypersensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; food hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis and eczema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis and eczema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (childhood) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; folate; hyperhomocystinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; folate; hyperhomocystinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma severity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mite-sensitive asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease mite-sensitive asthma 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.
asthma; allergic disease, ige mediated Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergic disease, ige mediated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. bhr. total ige. spt Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. bhr. total ige. spt in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma and ige in childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma and ige in childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; respiratory hypersensitivity; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; respiratory hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity, immediate Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity, immediate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aspirin-induced asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease aspirin-induced asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchiolitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchiolitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allergic diseases (bronchial asthma. atopic dermatitis and/or food-related anaphylaxis) Gene Set From GAD Gene-Disease Associations genes associated with the disease allergic diseases (bronchial asthma. atopic dermatitis and/or food-related anaphylaxis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis and eczema; anaphylaxis, food-related Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis and eczema; anaphylaxis, food-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; tremor Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. atopy. atopic dermatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. atopy. atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; asthma; diabetes, type 1; pemphigus; il-1ri Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; asthma; diabetes, type 1; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
steroid-requiring asthma in sedentary women Gene Set From GAD Gene-Disease Associations genes associated with the disease steroid-requiring asthma in sedentary women in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchial hyperreactivity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchial hyperreactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. total ige Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. total ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; atopic dermatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allergic conjunctivitis; asthma; conjunctivitis, allergic; dermatitis, atopic; eczema allergic; hypersensitivity; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease allergic conjunctivitis; asthma; conjunctivitis, allergic; dermatitis, atopic; eczema allergic; hypersensitivity; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ykl-40 levels ; asthma ; lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease ykl-40 levels ; asthma ; lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; urticaria Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; urticaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma eczema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma eczema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease ; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease ; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allergic asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease allergic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; pneumonia Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. allergy. Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. allergy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; recurrence; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; recurrence; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchial hyperreactivity; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchial hyperreactivity; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; hypersensitivity, immediate; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; hypersensitivity, immediate; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; autoimmune diseases; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; autoimmune diseases; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chromosome inversion; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chromosome inversion; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonatopic asthma and food allergy Gene Set From GAD Gene-Disease Associations genes associated with the disease nonatopic asthma and food allergy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergies Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchiolitis, viral; respiratory syncytial virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchiolitis, viral; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; bronchiectasis Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; bronchiectasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (childhood onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma. fev1 Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma. fev1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hypersensitivity; hypersensitivity, immediate; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity; hypersensitivity, immediate; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; allergen sensitization Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; allergen sensitization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; eczema; allergic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; eczema; allergic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term asthma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Asthma, allergic_Lung Tissue_GSE3184 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Asthma, allergic_Lung Tissue_GSE3184 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Asthma, allergic_Bronchial epithelium_GSE3004 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Asthma, allergic_Bronchial epithelium_GSE3004 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Asthma (toluene diisocyanate-induced) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (toluene diisocyanate-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma and hay fever Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma and hay fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to inhaled corticosteroid treatment in asthma (percentage change of FEV1) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to inhaled corticosteroid treatment in asthma (percentage change of FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (corticosteroid response) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (corticosteroid response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (sex interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (sex interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bronchodilator response in asthma (inhaled corticosteroid treatment interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bronchodilator response in asthma (inhaled corticosteroid treatment interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood, severe) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (bronchodilator response) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (bronchodilator response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
asthma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease asthma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
aspirin-induced asthma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aspirin-induced asthma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
asthma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the asthma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
asthma Gene Set From HPO Gene-Disease Associations genes associated with the asthma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aspirin-induced asthma Gene Set From HPO Gene-Disease Associations genes associated with the aspirin-induced asthma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Asthma, Aspirin-Induced Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Asthma, Aspirin-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Asthma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Asthma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Asthma, Exercise-Induced Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Asthma, Exercise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{asthma, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma susceptibility 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma susceptibility 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, nocturnal, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, nocturnal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, diminished response to antileukotriene treatment in} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, diminished response to antileukotriene treatment in} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma-related traits, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma-related traits, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, aspirin-induced, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, aspirin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma-related traits, susceptibility to, 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma-related traits, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma-related traits, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma-related traits, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma-related traits, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma-related traits, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{asthma-related traits, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {asthma-related traits, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{?allergy and asthma susceptibility} Gene Set From OMIM Gene-Disease Associations genes associated with the {?allergy and asthma susceptibility} phenotype from the curated OMIM Gene-Disease Associations dataset.
asthma and nasal polyps Gene Set From OMIM Gene-Disease Associations genes associated with the asthma and nasal polyps phenotype from the curated OMIM Gene-Disease Associations dataset.
Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Allergic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Allergic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ige-Mediated Allergic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ige-Mediated Allergic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asthma With Copd Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asthma With Copd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Onset Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Onset Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bakers' Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bakers' Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chemical-Induced Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chemical-Induced Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Obstructive Asthma (With Obstructive Pulmonary Disease) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Obstructive Asthma (With Obstructive Pulmonary Disease) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutrophilic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutrophilic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paucigranulocytic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paucigranulocytic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Allergic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Allergic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrinsic Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrinsic Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asa Intolerant Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asa Intolerant Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Moderate Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Moderate Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Onset Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Onset Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Asthma With Fungal Sensitisation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Asthma With Fungal Sensitisation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Severe Refractory Exacerbation Of Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Severe Refractory Exacerbation Of Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Allergic Rhinitis With Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Allergic Rhinitis With Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Induced Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Induced Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cough Variant Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cough Variant Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asthma Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atopic Asthma, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atopic Asthma, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Asthma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Asthma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Asthma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Asthma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrinsic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrinsic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Allergic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Allergic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrinsic asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrinsic asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Occupational asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Occupational asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Environmental induced asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Environmental induced asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
T2-low asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T2-low asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
T2-high asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T2-high asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
adult-onset severe asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease adult-onset severe asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nocturnal asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nocturnal asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intermittent asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermittent asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cough variant asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cough variant asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent severe asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent severe asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
asthma, nasal polyps, and aspirin intolerance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease asthma, nasal polyps, and aspirin intolerance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thunderstorm triggered asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thunderstorm triggered asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
near-fatal asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease near-fatal asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent moderate asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent moderate asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent mild asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent mild asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asthma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Asthma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited susceptibility to asthma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited susceptibility to asthma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adverse response to inhaled corticosteroid treatment x age interaction in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to inhaled corticosteroid treatment x age interaction in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever and/or eczema) (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to montelukast in asthma (change in FEV1) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to montelukast in asthma (change in FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to inhaled glucocorticoid treatment in asthma (change in FEV1) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to inhaled glucocorticoid treatment in asthma (change in FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to zileuton treatment in asthma (FEV1 change interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to zileuton treatment in asthma (FEV1 change interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral accretion in asthma (oral corticosteroid dose interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral accretion in asthma (oral corticosteroid dose interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever or eczema) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever or eczema) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Post-bronchodilator lung function in asthma (FVC) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator lung function in asthma (FVC) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lung function (FVC) in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function (FVC) in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Post-bronchodilator lung function in asthma (FEV1/FVC) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator lung function in asthma (FEV1/FVC) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Complete remission in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complete remission in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (moderate or severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (moderate or severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (adult onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (adult onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma onset (childhood vs adult) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma onset (childhood vs adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (corticosteroid response) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (corticosteroid response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (sex interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (sex interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to inhaled corticosteroid treatment in asthma (change in FEV1) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to inhaled corticosteroid treatment in asthma (change in FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bronchodilator response in asthma (inhaled corticosteroid treatment interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bronchodilator response in asthma (inhaled corticosteroid treatment interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma and hay fever Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and hay fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic rhinitis in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic rhinitis in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bronchodilator response in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bronchodilator response in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diisocyanate-induced asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diisocyanate-induced asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adult asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adult asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma-chronic obstructive pulmonary disease overlap syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma-chronic obstructive pulmonary disease overlap syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) x early life tobacco smoke interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) x early life tobacco smoke interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (bronchodilator response) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (bronchodilator response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (toluene diisocyanate-induced) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (toluene diisocyanate-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to mepolizumab in severe asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to mepolizumab in severe asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to placebo treatment in childhood asthma (FVC change) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to placebo treatment in childhood asthma (FVC change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma exacerbations in inhaled corticosteroid treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma exacerbations in inhaled corticosteroid treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Self-reported childhood asthma in adult smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported childhood asthma in adult smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe exacerbations in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma and eczema Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and eczema phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bronchial hyperresponsiveness in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bronchial hyperresponsiveness in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma or allergic disease (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma or allergic disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma and attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma and major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma Gene Set From KEGG Pathways 2026 proteins participating in the Asthma pathway from the KEGG Pathways 2026 dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation with infantile enterocolitis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation with infantile enterocolitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Galactosialidosis, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine palmitoyltransferase II deficiency, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type II, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked infantile nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile myofibromatosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile myofibromatosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amish infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Galactosialidosis, early infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyloric stenosis, infantile hypertrophic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Metachromatic leukodystrophy, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metachromatic leukodystrophy, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal neurodegeneration with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal neurodegeneration with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease, infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Liver failure acute infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Liver failure acute infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sting-associated vasculopathy, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sialic acid storage disease, severe infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune disease, multisystem, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinsonism-Dystonia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Hereditary spastic paralysis, infantile onset ascending Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.
Ceroid lipofuscinosis, neuronal 1, infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.
Infantile polyarteritis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infantile polyarteritis from the curated CTD Gene-Disease Associations dataset.
LIVER FAILURE, INFANTILE, TRANSIENT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LIVER FAILURE, INFANTILE, TRANSIENT from the curated CTD Gene-Disease Associations dataset.
Refsum Disease, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.
Glaucoma 3, primary infantile, B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amish Infantile Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.
Hemangioma, capillary infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemangioma, capillary infantile from the curated CTD Gene-Disease Associations dataset.
Striatonigral degeneration infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 5 from the curated CTD Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spasms, Infantile from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.
Hypophosphatasia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Infantile from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
infantile refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal infantile encephalocardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal infantile encephalocardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neurofibromatosis 1; spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease neurofibromatosis 1; spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypophosphatasia Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypophosphatasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variant late infantile neuronal ceroid lipofuscinosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile-onset ascending hereditary spastic paralysis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term infantile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
calcific stippling of infantile cartilaginous skeleton Gene Set From HPO Gene-Disease Associations genes associated with the calcific stippling of infantile cartilaginous skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile onset Gene Set From HPO Gene-Disease Associations genes associated with the infantile onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile hypercalcemia Gene Set From HPO Gene-Disease Associations genes associated with the infantile hypercalcemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile spasms Gene Set From HPO Gene-Disease Associations genes associated with the infantile spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile axial hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile axial hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spasms, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infantile Apparent Life-Threatening Event Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infantile Apparent Life-Threatening Event phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Diarrhea, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Diarrhea, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
pyloric stenosis, infantile hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 24 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 25 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 26 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 23 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
amish infantile epilepsy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the amish infantile epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertriglyceridemia, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypertriglyceridemia, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
liver failure, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the liver failure, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
?myofibromatosis, infantile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?myofibromatosis, infantile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercalcemia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypercalcemia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
nephronophthisis 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the nephronophthisis 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myofibromatosis, infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myofibromatosis, infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuroaxonal neurodegeneration, infantile, with facial dysmophism Gene Set From OMIM Gene-Disease Associations genes associated with the neuroaxonal neurodegeneration, infantile, with facial dysmophism phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinsonism-dystonia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
sting-associated vasculopathy, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
{hemangioma, capillary infantile, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hemangioma, capillary infantile, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus, infantile periodic alternating, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
hemangioma, capillary infantile, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the hemangioma, capillary infantile, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, infantile, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
?epileptic encephalopathy, early infantile, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set From OMIM Gene-Disease Associations genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypophosphatasia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatasia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
juvenile polyposis syndrome, infantile form Gene Set From OMIM Gene-Disease Associations genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
sandhoff disease, infantile, juvenile, and adult forms Gene Set From OMIM Gene-Disease Associations genes associated with the sandhoff disease, infantile, juvenile, and adult forms phenotype from the curated OMIM Gene-Disease Associations dataset.
sialic acid storage disorder, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the sialic acid storage disorder, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
autoinflammation with infantile enterocolitis Gene Set From OMIM Gene-Disease Associations genes associated with the autoinflammation with infantile enterocolitis phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune disease, multisystem, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set From OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.
striatonigral degeneration, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
glaucoma 3, primary infantile, b Gene Set From OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary infantile, b phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paralysis, infantile onset ascending Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.
Infantile Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Spasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Spasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Nystagmus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Nystagmus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Myofibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Myofibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Infantile Neuronal Ceroid Lipfuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Infantile Neuronal Ceroid Lipfuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Severe Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Severe Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Scurvy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Scurvy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Infantile Neurological, Cutaneous, And Articular Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy With Suppression Bursts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy With Suppression Bursts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hypophosphatasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hypophosphatasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemangioma, Capillary Infantile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemangioma, Capillary Infantile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration, Infantile, Mitochondrial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration, Infantile, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Malignant Osteopetrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Malignant Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endemic Tyrolean Infantile Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Endemic Tyrolean Infantile Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amish Infantile Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Encephalopathy, Infantile Subacute, Of Leigh in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Infantile Nystagmus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Refsum Disease (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Refsum Disease (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Infantile Myasthenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Onset Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Onset Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystinosis, Infantile Nephropathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystinosis, Infantile Nephropathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fastkd2-Related Infantile Mitochondrial Encephalomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fastkd2-Related Infantile Mitochondrial Encephalomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Atopic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Globoid Cell Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Globoid Cell Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sandhoff Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sandhoff Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sting-Associated Vasculopathy, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sting-Associated Vasculopathy, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Digital Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Digital Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Liver Failure Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Liver Failure Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Constant Exotropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Constant Exotropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gm 2 Gangliosidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gm 2 Gangliosidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Infantile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Infantile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monoplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monoplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gastroenteritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Infantile Mitochondrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Infantile Mitochondrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Free Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Free Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma And Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma And Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver Failure, Infantile, Transient Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver Failure, Infantile, Transient in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Diarrhea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Nystagmus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Obesity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Axial Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Axial Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hemangioma, Capillary Infantile, Somatic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hemangioma, Capillary Infantile, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Colic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Colic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 pathway from the Reactome Pathways 2024 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 pathway from the Reactome Pathways 2024 dataset.
COX deficiency, infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early infantile epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early infantile epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile Refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile Refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile parkinsonism-dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile parkinsonism-dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypophosphatasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile myofibromatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile myofibromatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient infantile liver failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient infantile liver failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypotonia with psychomotor retardation and characteristic facies-3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypotonia with psychomotor retardation and characteristic facies-3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile histiocytoid cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile histiocytoid cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-infantile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-infantile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic infantile neurological Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic infantile neurological phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile onset spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile onset spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal/infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal/infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Capillary infantile hemangioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary infantile hemangioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign sporadic infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign sporadic infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LAMB2-related infantile-onset nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LAMB2-related infantile-onset nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephropathic cystinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephropathic cystinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile spasms Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile spasms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile convulsions and choreoathetosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile convulsions and choreoathetosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile myofibromatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile myofibromatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile Nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile Nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Self-limited familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early Infantile Epileptic Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early Infantile Epileptic Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal Infantile Cardioencephalomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal Infantile Cardioencephalomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Periodic fever-infantile enterocolitis-autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever-infantile enterocolitis-autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile osteopetrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile osteopetrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic Infantile Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic Infantile Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IL21-related infantile inflammatory bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IL21-related infantile inflammatory bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epileptic dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epileptic dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile or childhood onset neurodegenerative disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset generalized dyskinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset generalized dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient infantile hypertriglyceridemia and hepatosteatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient infantile hypertriglyceridemia and hepatosteatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic kinesigenic dyskinesia and familial infantile convulsions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia and familial infantile convulsions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

BFIS1 Gene

NYS5 Gene

CLN6 Gene

BFIS4 Gene

PKDTS Gene

BFIC2 Gene

EIM Gene

GLC3B Gene

IHPS2 Gene

CMS1A1 Gene

IHPS5 Gene

IHPS4 Gene

IHPS3 Gene

Infantile Asthma Gene Set

asthma. asthma severity Gene Set

Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 Gene Set

Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set

Asthma, Aspirin-Induced Gene Set

Asthma Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 Gene Set

Asthma, Exercise-Induced Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Gene Set

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 Gene Set

Asthma Gene Set

asthma Gene Set

asthma Gene Set

intrinsic asthma Gene Set

asthma Gene Set

cough variant asthma Gene Set

allergic asthma Gene Set

asthma; dermatitis, atopic; Gene Set

ascariasis; asthma; Gene Set

asthma; ige Gene Set

asthma; recurrence; respiratory sounds; respiratory syncytial virus infections Gene Set

asthma; prenatal exposure delayed effects; respiratory sounds Gene Set

asthma; drug hypersensitivity; Gene Set

asthma; occupational diseases Gene Set

asthma; hypersensitivity Gene Set

asthma; drug hypersensitivity; hypersensitivity, immediate; urticaria Gene Set

asthma and atopy Gene Set

asthma; allergy Gene Set

bronchial asthma Gene Set

asthma; atopy; dermatitis and eczema Gene Set

asthma; eczema; food hypersensitivity; hypersensitivity, immediate; respiratory sounds; rhinitis, allergic, seasonal Gene Set

asthma; eosinophilia Gene Set

asthma; hypersensitivity, immediate; recurrence Gene Set

asthma; nasal polyps Gene Set

asthma; conjunctivitis, allergic; hypersensitivity; rhinitis Gene Set

asthma; respiratory sounds Gene Set

ulcerative colitis; asthma Gene Set

crohn's disease; asthma; malaria Gene Set

asthma; familial mediterranean fever Gene Set

asthma; dermatitis, atopic; rhinitis, allergic Gene Set

asthma; dermatitis, atopic; egg hypersensitivity; food hypersensitivity Gene Set

myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd Gene Set

asthma; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set

asthma; hypersensitivity; respiratory tract infections Gene Set

asthma; hypersensitivity; occupational diseases Gene Set

asthma, aspirin-induced; urticaria, aspirin-intolerant Gene Set

childhood asthma Gene Set

asthma; dermatitis, atopic; eczema; rhinitis, allergic, seasonal Gene Set

asthma. rhinitis Gene Set

asthma; respiratory tract infections Gene Set

bronchial asthma (childhood only) Gene Set

asthma; helicobacter infections; hypersensitivity, immediate Gene Set

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

asthma. atopy Gene Set

asthma; candidiasis; high-altitude illness Gene Set

asthma; drug therapy; Gene Set

lung cancer; asthma; emphysema; bronchitis; pneumonia; hay fever Gene Set

asthma; rhinitis Gene Set

lung cancer; asthma Gene Set

asthma (toluene diisocyanate-induced) Gene Set

asthma; tuberculosis Gene Set