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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06139FOXA3stomachMESH:D003924Diabetes Mellitus, Type 2pancreas
HM06139FOXA3stomachMESH:D001848Bone Diseases, Developmental
HM06139FOXA3stomachMESH:D006470Hemorrhage
HM06139FOXA3stomachMESH:D008064Lipidoses
HM06139FOXA3stomachMESH:D006943Hyperglycemia
HM06139FOXA3stomachMESH:D010190Pancreatic Neoplasmspancreas
HM06139FOXA3stomachMESH:D007248Infertility, Male
HM06139FOXA3stomachMESH:D017114Liver Failure, Acute
HM06139FOXA3stomachMESH:D013276Stomach Ulcer
HM06139FOXA3stomachMESH:D013971Thyrotoxicosisthyroid
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseasesspinal cord
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseasesskin
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseasesnerve
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseasesmuscle
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseaseseye
HM06139FOXA3stomachMESH:D002493Central Nervous System Diseasesbrain
HM06139FOXA3stomachMESH:D008546Melanoma, Experimental
HM06139FOXA3stomachMESH:D001281Atrial Fibrillation
HM06139FOXA3stomachMESH:D004489Edema, Cardiac
HM06139FOXA3stomachMESH:D008113Liver Neoplasms
HM06139FOXA3stomachMESH:D008113Liver Neoplasms
HM06139FOXA3stomachMESH:D005313Fetal Death
HM06139FOXA3stomachMESH:D018281Cholangiocarcinomaliver
HM06139FOXA3stomachMESH:D003876Dermatitis, Atopicskin
HM06139FOXA3stomachMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06139FOXA3stomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM06139FOXA3stomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM06139FOXA3stomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM06139FOXA3stomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM06139FOXA3stomachMESH:D009181Mycoses
HM06139FOXA3stomachMESH:D000740Anemiabone marrow
HM06139FOXA3stomachMESH:D019851Thrombophiliabone marrow
HM06139FOXA3stomachMESH:D001145Arrhythmias, Cardiac
HM06139FOXA3stomachMESH:D000013Congenital Abnormalities
HM06139FOXA3stomachMESH:D005124Eye Abnormalities
HM06139FOXA3stomachMESH:D014605Uveitiseye
HM06139FOXA3stomachMESH:D000152Acne Vulgaris
HM06139FOXA3stomachMESH:D006330Heart Defects, Congenital
HM06139FOXA3stomachMESH:D008107Liver Diseasesskin
HM06139FOXA3stomachMESH:D008107Liver Diseasesmuscle
HM06139FOXA3stomachMESH:D008107Liver Diseaseslung
HM06139FOXA3stomachMESH:D008107Liver Diseasesliver
HM06139FOXA3stomachMESH:D011658Pulmonary Fibrosislung
HM06139FOXA3stomachMESH:D015619Respiratory System Abnormalities
HM06139FOXA3stomachMESH:D055371Acute Lung Injury
HM06139FOXA3stomachMESH:D004362Drug Toxicity
HM06139FOXA3stomachMESH:D006332Cardiomegaly
HM06139FOXA3stomachMESH:D006529Hepatomegaly
HM06139FOXA3stomachMESH:D003294Seizures, Febrile
HM06139FOXA3stomachMESH:D013088Spermatocele
HM06139FOXA3stomachMESH:D007674Kidney Diseasesureter
HM06139FOXA3stomachMESH:D007674Kidney Diseasespituitary
HM06139FOXA3stomachMESH:D007674Kidney Diseaseskidney
HM06139FOXA3stomachMESH:D007333Insulin Resistance
HM06139FOXA3stomachMESH:D007638Keratoconjunctivitis Siccaeye
HM06139FOXA3stomachMESH:D009421Nervous System Malformations
HM06139FOXA3stomachMESH:D009765Obesity
HM06139FOXA3stomachMESH:D019310Pseudolymphoma
HM06139FOXA3stomachMESH:D013927Thrombosis
HM06139FOXA3stomachMESH:D010146Pain
HM06139FOXA3stomachMESH:D002277Carcinoma
HM06139FOXA3stomachMESH:D002386Cataractpancreas
HM06139FOXA3stomachMESH:D002386Cataracteye
HM06139FOXA3stomachMESH:D005355Fibrosis
HM06139FOXA3stomachMESH:D017119Porphyria Cutanea Tardaskin
HM06139FOXA3stomachMESH:D014985Xerophthalmiaeye
HM06139FOXA3stomachMESH:D056486Drug-Induced Liver Injury
HM06139FOXA3stomachMESH:D006937Hypercholesterolemia
HM06139FOXA3stomachMESH:D009369Neoplasmsspleen
HM06139FOXA3stomachMESH:D009369Neoplasmsbone marrow
HM06139FOXA3stomachMESH:D012878Skin Neoplasms
HM06139FOXA3stomachMESH:D002972Cleft Palate
HM06139FOXA3stomachMESH:D004828Epilepsies, Partialmuscle
HM06139FOXA3stomachMESH:D015427Reperfusion Injury
HM06139FOXA3stomachMESH:D000014Abnormalities, Drug-Induced
HM06139FOXA3stomachMESH:D002779Cholestasisliver
HM06139FOXA3stomachMESH:D006457Hemoglobinuria, Paroxysmal
HM06139FOXA3stomachMESH:D006930Hyperalgesia
HM06139FOXA3stomachMESH:D008171Lung Diseases
HM06139FOXA3stomachMESH:D017180Tachycardia, Ventricular
HM06139FOXA3stomachMESH:D006333Heart Failureheart
HM06139FOXA3stomachMESH:D007249Inflammation
HM06139FOXA3stomachMESH:D008106Liver Cirrhosis, Experimental
HM06139FOXA3stomachMESH:D016584Panic Disorder
HM06139FOXA3stomachMESH:D007569Jaw Abnormalities
HM06139FOXA3stomachMESH:D007037Hypothyroidismthyroid
HM06139FOXA3stomachMESH:D011297Prenatal Exposure Delayed Effects
HM06139FOXA3stomachMESH:D008114Liver Neoplasms, Experimental
HM06139FOXA3stomachMESH:D008133Long QT Syndrome
HM06139FOXA3stomachMESH:D019465Craniofacial Abnormalities
HM06139FOXA3stomachMESH:D004827Epilepsymuscle
HM06139FOXA3stomachMESH:D009203Myocardial Infarctionheart
HM06139FOXA3stomachMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM06139FOXA3stomachMESH:D004421Dystonia
HM06139FOXA3stomachMESH:D000230Adenocarcinoma
HM06139FOXA3stomachMESH:D000230Adenocarcinomauterus
HM06139FOXA3stomachMESH:D000230Adenocarcinoma
HM06139FOXA3stomachMESH:D000230Adenocarcinoma
HM06139FOXA3stomachMESH:D000230Adenocarcinomauterus
HM06139FOXA3stomachMESH:D000230Adenocarcinomathyroid
HM06139FOXA3stomachMESH:D000230Adenocarcinomaskin
HM06139FOXA3stomachMESH:D000230Adenocarcinomaparathyroid gland
HM06139FOXA3stomachMESH:D000230Adenocarcinomaliver
HM06139FOXA3stomachMESH:D000230Adenocarcinomakidney
HM06139FOXA3stomachMESH:D000230Adenocarcinomaeye
HM06139FOXA3stomachMESH:D000230Adenocarcinomaadrenal gland
HM06139FOXA3stomachMESH:D004831Epilepsies, Myoclonicmuscle
HM06139FOXA3stomachMESH:D005885Gingival Hyperplasia
HM06139FOXA3stomachMESH:D006973Hypertensionlung
HM06139FOXA3stomachMESH:D006973Hypertensionheart
HM06139FOXA3stomachMESH:D006973Hypertensionblood vessel
HM06139FOXA3stomachMESH:D006528Carcinoma, Hepatocellularliver
HM06139FOXA3stomachMESH:D002311Cardiomyopathy, Dilatedheart
HM06139FOXA3stomachMESH:D019636Neurodegenerative Diseasesnerve
HM06139FOXA3stomachMESH:D014594Uterine Neoplasmscervix
HM06139FOXA3stomachMESH:D014594Uterine Neoplasms
HM06139FOXA3stomachMESH:D005234Fatty Liver
HM06139FOXA3stomachMESH:D008569Memory Disorders
HM06139FOXA3stomachMESH:D011230Precancerous Conditions
HM06139FOXA3stomachMESH:D020191Myoclonic Epilepsies, Progressivenerve
HM06139FOXA3stomachMESH:D020191Myoclonic Epilepsies, Progressivemuscle
HM06139FOXA3stomachMESH:D004832Epilepsy, Absencemuscle
HM06139FOXA3stomachOMIM:609620SHORT QT SYNDROME 1
HM06139FOXA3stomachMESH:D001161Arteriosclerosisblood vessel
HM06139FOXA3stomachMESH:D007247Infertility, Female
HM06139FOXA3stomachMESH:D013959Thyroid Diseasesthyroid
HM06139FOXA3stomachMESH:D007021Hypospadias
HM06139FOXA3stomachMESH:D001778Blood Coagulation Disordersbone marrow
HM06139FOXA3stomachMESH:D010382Peliosis Hepatisliver
HM06139FOXA3stomachMESH:D019282Wasting Syndrome
HM06139FOXA3stomachMESH:D000799Angioedemaskin
HM06139FOXA3stomachMESH:D014581Urticariaskin
HM06139FOXA3stomachMESH:D017563Lung Diseases, Interstitiallung
HM06139FOXA3stomachMESH:D008175Lung Neoplasmslung
HM06139FOXA3stomachMESH:D017202Myocardial Ischemiaheart
HM06139FOXA3stomachMESH:D011565Psoriasisskin
HM06139FOXA3stomachMESH:D002341Carotid Artery Thrombosisblood vessel
HM06139FOXA3stomachMESH:D004487Edema
HM06139FOXA3stomachMESH:D009402Nephrosis, Lipoidkidney
HM06139FOXA3stomachMESH:D001169Arthritis, Experimental
HM06139FOXA3stomachMESH:D001943Breast Neoplasmsbreast
HM06139FOXA3stomachMESH:D007859Learning Disorders
HM06139FOXA3stomachMESH:D009404Nephrotic Syndromekidney
HM06139FOXA3stomachMESH:D010018Osteomalaciabone
HM06139FOXA3stomachMESH:D011537Pruritus
HM06139FOXA3stomachMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM06139FOXA3stomachMESH:D009135Muscular Diseasesmuscle
HM06139FOXA3stomachMESH:D018248Adenoma, Liver Cell
HM06139FOXA3stomachMESH:D001321Autistic Disorder
HM06139FOXA3stomachMESH:D015428Myocardial Reperfusion Injury
HM06139FOXA3stomachMESH:D001836Body Weight Changes
HM06139FOXA3stomachMESH:D016171Torsades de Pointes
HM06139FOXA3stomachMESH:D020246Venous Thrombosis
HM06139FOXA3stomachMESH:D017029Epilepsy, Complex Partialmuscle
HM06139FOXA3stomachMESH:D006869Hydronephrosiskidney
HM06139FOXA3stomachMESH:D012640Seizuresmuscle
HM06139FOXA3stomachMESH:D054079Vascular Malformations
HM06139FOXA3stomachMESH:D013610Tachycardia