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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00391EGFL6placentaMESH:D030342Genetic Diseases, Inborn
HM00391EGFL6placentaMESH:D011472Prostatitisprostate
HM00391EGFL6placentaMESH:D011658Pulmonary Fibrosislung
HM00391EGFL6placentaMESH:D013276Stomach Ulcer
HM00391EGFL6placentaMESH:D007248Infertility, Male
HM00391EGFL6placentaMESH:D007984Leydig Cell Tumor
HM00391EGFL6placentaMESH:D001008Anxiety Disorders
HM00391EGFL6placentaMESH:D003456Cryptorchidism
HM00391EGFL6placentaMESH:D001281Atrial Fibrillation
HM00391EGFL6placentaMESH:D007037Hypothyroidismthyroid
HM00391EGFL6placentaMESH:D008133Long QT Syndrome
HM00391EGFL6placentaMESH:D017180Tachycardia, Ventricular
HM00391EGFL6placentaMESH:D006529Hepatomegaly
HM00391EGFL6placentaMESH:D013971Thyrotoxicosisthyroid
HM00391EGFL6placentaMESH:D016171Torsades de Pointes
HM00391EGFL6placentaMESH:D056486Drug-Induced Liver Injury
HM00391EGFL6placentaMESH:D013959Thyroid Diseasesthyroid
HM00391EGFL6placentaMESH:D008064Lipidoses
HM00391EGFL6placentaMESH:D002311Cardiomyopathy, Dilatedheart
HM00391EGFL6placentaMESH:D001145Arrhythmias, Cardiac
HM00391EGFL6placentaMESH:D009181Mycoses
HM00391EGFL6placentaMESH:D013610Tachycardia
HM00391EGFL6placentaMESH:D011297Prenatal Exposure Delayed Effects
HM00391EGFL6placentaOMIM:609620SHORT QT SYNDROME 1
HM00391EGFL6placentaMESH:D002341Carotid Artery Thrombosisblood vessel
HM00391EGFL6placentaMESH:D017563Lung Diseases, Interstitiallung
HM00391EGFL6placentaMESH:D008171Lung Diseases
HM00391EGFL6placentaMESH:D001778Blood Coagulation Disordersbone marrow
HM00391EGFL6placentaMESH:D006937Hypercholesterolemia
HM00391EGFL6placentaMESH:D011469Prostatic Diseasesureter
HM00391EGFL6placentaMESH:D011469Prostatic Diseasesprostate
HM00391EGFL6placentaMESH:D005234Fatty Liver
HM00391EGFL6placentaMESH:D005832Genital Diseases, Maletestis
HM00391EGFL6placentaMESH:D005832Genital Diseases, Maleprostate
HM00391EGFL6placentaMESH:D005832Genital Diseases, Maleblood vessel