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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02755SLITRK3brainMESH:D007037Hypothyroidismthyroid
HM02755SLITRK3brainMESH:D004487Edema
HM02755SLITRK3brainMESH:D017563Lung Diseases, Interstitiallung
HM02755SLITRK3brainMESH:D001008Anxiety Disorders
HM02755SLITRK3brainMESH:D006943Hyperglycemia
HM02755SLITRK3brainMESH:D001281Atrial Fibrillation
HM02755SLITRK3brainMESH:D013610Tachycardia
HM02755SLITRK3brainMESH:D017180Tachycardia, Ventricular
HM02755SLITRK3brainMESH:D001778Blood Coagulation Disordersbone marrow
HM02755SLITRK3brainMESH:D003456Cryptorchidism
HM02755SLITRK3brainMESH:D009203Myocardial Infarctionheart
HM02755SLITRK3brainMESH:D002341Carotid Artery Thrombosisblood vessel
HM02755SLITRK3brainMESH:D005832Genital Diseases, Maletestis
HM02755SLITRK3brainMESH:D005832Genital Diseases, Maleprostate
HM02755SLITRK3brainMESH:D005832Genital Diseases, Maleblood vessel
HM02755SLITRK3brainMESH:D007248Infertility, Male
HM02755SLITRK3brainMESH:D002311Cardiomyopathy, Dilatedheart
HM02755SLITRK3brainMESH:D006529Hepatomegaly
HM02755SLITRK3brainMESH:D008106Liver Cirrhosis, Experimental
HM02755SLITRK3brainMESH:D001145Arrhythmias, Cardiac
HM02755SLITRK3brainMESH:D006937Hypercholesterolemia
HM02755SLITRK3brainMESH:D007333Insulin Resistance
HM02755SLITRK3brainMESH:D056486Drug-Induced Liver Injury
HM02755SLITRK3brainMESH:D006333Heart Failureheart
HM02755SLITRK3brainMESH:D009135Muscular Diseasesmuscle
HM02755SLITRK3brainMESH:D009369Neoplasmsspleen
HM02755SLITRK3brainMESH:D009369Neoplasmsbone marrow
HM02755SLITRK3brainMESH:D009765Obesity
HM02755SLITRK3brainMESH:D013959Thyroid Diseasesthyroid
HM02755SLITRK3brainMESH:D055371Acute Lung Injury
HM02755SLITRK3brainMESH:D011297Prenatal Exposure Delayed Effects
HM02755SLITRK3brainMESH:D016171Torsades de Pointes
HM02755SLITRK3brainMESH:D013971Thyrotoxicosisthyroid
HM02755SLITRK3brainMESH:D008133Long QT Syndrome
HM02755SLITRK3brainMESH:D002779Cholestasisliver
HM02755SLITRK3brainMESH:D011472Prostatitisprostate
HM02755SLITRK3brainMESH:D011658Pulmonary Fibrosislung
HM02755SLITRK3brainMESH:D030342Genetic Diseases, Inborn
HM02755SLITRK3brainMESH:D015428Myocardial Reperfusion Injury
HM02755SLITRK3brainOMIM:609620SHORT QT SYNDROME 1
HM02755SLITRK3brainMESH:D011469Prostatic Diseasesureter
HM02755SLITRK3brainMESH:D011469Prostatic Diseasesprostate
HM02755SLITRK3brainMESH:D005234Fatty Liver
HM02755SLITRK3brainMESH:D008064Lipidoses
HM02755SLITRK3brainMESH:D003876Dermatitis, Atopicskin
HM02755SLITRK3brainMESH:D008113Liver Neoplasms
HM02755SLITRK3brainMESH:D008113Liver Neoplasms
HM02755SLITRK3brainMESH:D009181Mycoses
HM02755SLITRK3brainMESH:D007984Leydig Cell Tumor
HM02755SLITRK3brainMESH:D008171Lung Diseases
HM02755SLITRK3brainMESH:D018248Adenoma, Liver Cell
HM02755SLITRK3brainMESH:D015427Reperfusion Injury
HM02755SLITRK3brainMESH:D013276Stomach Ulcer