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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06584CNPbrainMESH:D008171Lung Diseases
HM06584CNPbrainMESH:D001778Blood Coagulation Disordersbone marrow
HM06584CNPbrainMESH:D056486Drug-Induced Liver Injury
HM06584CNPbrainMESH:D006529Hepatomegaly
HM06584CNPbrainMESH:D016171Torsades de Pointes
HM06584CNPbrainMESH:D002341Carotid Artery Thrombosisblood vessel
HM06584CNPbrainMESH:D017563Lung Diseases, Interstitiallung
HM06584CNPbrainMESH:D006970Disorders of Excessive Somnolence
HM06584CNPbrainMESH:D013971Thyrotoxicosisthyroid
HM06584CNPbrainMESH:D002311Cardiomyopathy, Dilatedheart
HM06584CNPbrainMESH:D017180Tachycardia, Ventricular
HM06584CNPbrainMESH:D003704Dementianerve
HM06584CNPbrainMESH:D003704Dementiablood vessel
HM06584CNPbrainMESH:D050171Dyslipidemias
HM06584CNPbrainOMIM:609620SHORT QT SYNDROME 1
HM06584CNPbrainMESH:D003924Diabetes Mellitus, Type 2pancreas
HM06584CNPbrainMESH:D008133Long QT Syndrome
HM06584CNPbrainMESH:D001523Mental Disorders
HM06584CNPbrainMESH:D011618Psychotic Disorders
HM06584CNPbrainMESH:D016757Death, Sudden, Cardiac
HM06584CNPbrainMESH:D015431Weight Loss
HM06584CNPbrainMESH:D001321Autistic Disorder
HM06584CNPbrainMESH:D011658Pulmonary Fibrosislung
HM06584CNPbrainMESH:D013610Tachycardia
HM06584CNPbrainMESH:D006937Hypercholesterolemia
HM06584CNPbrainMESH:D009181Mycoses
HM06584CNPbrainMESH:D005234Fatty Liver
HM06584CNPbrainMESH:D008064Lipidoses
HM06584CNPbrainMESH:D001281Atrial Fibrillation
HM06584CNPbrainMESH:D015430Weight Gain
HM06584CNPbrainMESH:D011595Psychomotor Agitation
HM06584CNPbrainMESH:D002375Catalepsy
HM06584CNPbrainMESH:D007037Hypothyroidismthyroid
HM06584CNPbrainMESH:D013959Thyroid Diseasesthyroid
HM06584CNPbrainMESH:D003072Cognition Disorders
HM06584CNPbrainMESH:D006948Hyperkinesis
HM06584CNPbrainMESH:D000380Agranulocytosisbone marrow
HM06584CNPbrainMESH:D013276Stomach Ulcer
HM06584CNPbrainMESH:D009765Obesity
HM06584CNPbrainMESH:D012559Schizophrenia
HM06584CNPbrainMESH:D024821Metabolic Syndrome X
HM06584CNPbrainMESH:D001145Arrhythmias, Cardiac