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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00023CPLX2brainMESH:D008325Mammary Neoplasms, Experimental
HM00023CPLX2brainMESH:D001778Blood Coagulation Disordersbone marrow
HM00023CPLX2brainMESH:D006948Hyperkinesis
HM00023CPLX2brainMESH:D013964Thyroid Neoplasmsthyroid
HM00023CPLX2brainMESH:D007247Infertility, Female
HM00023CPLX2brainMESH:D008171Lung Diseases
HM00023CPLX2brainMESH:D013733Testicular Diseasestestis
HM00023CPLX2brainMESH:D008654Mesotheliomabone
HM00023CPLX2brainMESH:D001714Bipolar Disorder
HM00023CPLX2brainMESH:D002418Cattle Diseases
HM00023CPLX2brainMESH:D011472Prostatitisprostate
HM00023CPLX2brainMESH:D050171Dyslipidemias
HM00023CPLX2brainMESH:D006529Hepatomegaly
HM00023CPLX2brainMESH:D007938Leukemiaspleen
HM00023CPLX2brainMESH:D007938Leukemiabone marrow
HM00023CPLX2brainMESH:D009422Nervous System Diseases
HM00023CPLX2brainMESH:D008064Lipidoses
HM00023CPLX2brainMESH:D017563Lung Diseases, Interstitiallung
HM00023CPLX2brainMESH:D010523Peripheral Nervous System Diseasesnerve
HM00023CPLX2brainMESH:D011469Prostatic Diseasesureter
HM00023CPLX2brainMESH:D011469Prostatic Diseasesprostate
HM00023CPLX2brainMESH:D011471Prostatic Neoplasmsprostate
HM00023CPLX2brainMESH:D015430Weight Gain
HM00023CPLX2brainMESH:D001281Atrial Fibrillation
HM00023CPLX2brainMESH:D011658Pulmonary Fibrosislung
HM00023CPLX2brainMESH:D003456Cryptorchidism
HM00023CPLX2brainMESH:D005832Genital Diseases, Maletestis
HM00023CPLX2brainMESH:D005832Genital Diseases, Maleprostate
HM00023CPLX2brainMESH:D005832Genital Diseases, Maleblood vessel
HM00023CPLX2brainMESH:D007248Infertility, Male
HM00023CPLX2brainMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00023CPLX2brainMESH:D006970Disorders of Excessive Somnolence
HM00023CPLX2brainMESH:D024821Metabolic Syndrome X
HM00023CPLX2brainMESH:D001943Breast Neoplasmsbreast
HM00023CPLX2brainMESH:D002311Cardiomyopathy, Dilatedheart
HM00023CPLX2brainMESH:D006937Hypercholesterolemia
HM00023CPLX2brainMESH:D009181Mycoses
HM00023CPLX2brainMESH:D009765Obesity
HM00023CPLX2brainMESH:D007037Hypothyroidismthyroid
HM00023CPLX2brainOMIM:609620SHORT QT SYNDROME 1
HM00023CPLX2brainMESH:D030342Genetic Diseases, Inborn
HM00023CPLX2brainMESH:D009410Nerve Degeneration
HM00023CPLX2brainMESH:D011618Psychotic Disorders
HM00023CPLX2brainMESH:D011297Prenatal Exposure Delayed Effects
HM00023CPLX2brainMESH:D002341Carotid Artery Thrombosisblood vessel
HM00023CPLX2brainMESH:D056486Drug-Induced Liver Injury
HM00023CPLX2brainMESH:D008133Long QT Syndrome
HM00023CPLX2brainMESH:D012135Respiratory Sounds
HM00023CPLX2brainMESH:D016171Torsades de Pointes
HM00023CPLX2brainMESH:D013959Thyroid Diseasesthyroid
HM00023CPLX2brainMESH:D001145Arrhythmias, Cardiac
HM00023CPLX2brainMESH:D015431Weight Loss
HM00023CPLX2brainMESH:D013971Thyrotoxicosisthyroid
HM00023CPLX2brainMESH:D003072Cognition Disorders
HM00023CPLX2brainMESH:D005234Fatty Liver
HM00023CPLX2brainMESH:D017449Dermatitis, Allergic Contactskin
HM00023CPLX2brainMESH:D017180Tachycardia, Ventricular
HM00023CPLX2brainMESH:D009101Multiple Myelomabone marrow
HM00023CPLX2brainMESH:D012559Schizophrenia
HM00023CPLX2brainMESH:D001008Anxiety Disorders
HM00023CPLX2brainMESH:D001523Mental Disorders
HM00023CPLX2brainMESH:D009669Nose Neoplasms
HM00023CPLX2brainMESH:D013276Stomach Ulcer
HM00023CPLX2brainMESH:D007984Leydig Cell Tumor
HM00023CPLX2brainMESH:D000380Agranulocytosisbone marrow
HM00023CPLX2brainMESH:D000382Agricultural Workers' Diseases
HM00023CPLX2brainMESH:D013610Tachycardia