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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04711PRR15colonMESH:D007249Inflammation
HM04711PRR15colonMESH:D006332Cardiomegaly
HM04711PRR15colonMESH:D015428Myocardial Reperfusion Injury
HM04711PRR15colonMESH:D010382Peliosis Hepatisliver
HM04711PRR15colonMESH:D008106Liver Cirrhosis, Experimental
HM04711PRR15colonMESH:D054079Vascular Malformations
HM04711PRR15colonMESH:D001848Bone Diseases, Developmental
HM04711PRR15colonMESH:D009369Neoplasmsspleen
HM04711PRR15colonMESH:D009369Neoplasmsbone marrow
HM04711PRR15colonMESH:D018281Cholangiocarcinomaliver
HM04711PRR15colonMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04711PRR15colonMESH:D011297Prenatal Exposure Delayed Effects
HM04711PRR15colonMESH:D004487Edema
HM04711PRR15colonMESH:D006973Hypertensionlung
HM04711PRR15colonMESH:D006973Hypertensionheart
HM04711PRR15colonMESH:D006973Hypertensionblood vessel
HM04711PRR15colonMESH:D017202Myocardial Ischemiaheart
HM04711PRR15colonMESH:D015619Respiratory System Abnormalities
HM04711PRR15colonMESH:D013959Thyroid Diseasesthyroid
HM04711PRR15colonMESH:D002779Cholestasisliver
HM04711PRR15colonMESH:D002972Cleft Palate
HM04711PRR15colonMESH:D005313Fetal Death
HM04711PRR15colonMESH:D005124Eye Abnormalities
HM04711PRR15colonMESH:D008113Liver Neoplasms
HM04711PRR15colonMESH:D008113Liver Neoplasms
HM04711PRR15colonMESH:D019465Craniofacial Abnormalities
HM04711PRR15colonMESH:D000740Anemiabone marrow
HM04711PRR15colonMESH:D003876Dermatitis, Atopicskin
HM04711PRR15colonMESH:D008114Liver Neoplasms, Experimental
HM04711PRR15colonMESH:D009135Muscular Diseasesmuscle
HM04711PRR15colonMESH:D004489Edema, Cardiac
HM04711PRR15colonMESH:D006470Hemorrhage
HM04711PRR15colonMESH:D018248Adenoma, Liver Cell
HM04711PRR15colonMESH:D000013Congenital Abnormalities
HM04711PRR15colonMESH:D007569Jaw Abnormalities
HM04711PRR15colonMESH:D055371Acute Lung Injury
HM04711PRR15colonMESH:D006943Hyperglycemia
HM04711PRR15colonMESH:D002277Carcinoma
HM04711PRR15colonMESH:D004362Drug Toxicity
HM04711PRR15colonMESH:D005234Fatty Liver
HM04711PRR15colonMESH:D017119Porphyria Cutanea Tardaskin
HM04711PRR15colonMESH:D001943Breast Neoplasmsbreast
HM04711PRR15colonMESH:D005355Fibrosis
HM04711PRR15colonMESH:D008175Lung Neoplasmslung
HM04711PRR15colonMESH:D009203Myocardial Infarctionheart
HM04711PRR15colonMESH:D001778Blood Coagulation Disordersbone marrow
HM04711PRR15colonMESH:D015427Reperfusion Injury
HM04711PRR15colonMESH:D001836Body Weight Changes
HM04711PRR15colonMESH:D002471Cell Transformation, Neoplastic
HM04711PRR15colonMESH:D056486Drug-Induced Liver Injury
HM04711PRR15colonMESH:D006330Heart Defects, Congenital
HM04711PRR15colonMESH:D019282Wasting Syndrome
HM04711PRR15colonMESH:D006529Hepatomegaly
HM04711PRR15colonMESH:D006869Hydronephrosiskidney
HM04711PRR15colonMESH:D004938Esophageal Neoplasms
HM04711PRR15colonMESH:D009765Obesity
HM04711PRR15colonMESH:D012878Skin Neoplasms
HM04711PRR15colonMESH:D007333Insulin Resistance
HM04711PRR15colonMESH:D006333Heart Failureheart
HM04711PRR15colonMESH:D009421Nervous System Malformations
HM04711PRR15colonMESH:D000014Abnormalities, Drug-Induced