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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05737PTDSS1lymphMESH:D007248Infertility, Male
HM05737PTDSS1lymphMESH:D007333Insulin Resistance
HM05737PTDSS1lymphMESH:D008113Liver Neoplasms
HM05737PTDSS1lymphMESH:D008113Liver Neoplasms
HM05737PTDSS1lymphMESH:D002779Cholestasisliver
HM05737PTDSS1lymphMESH:D004489Edema, Cardiac
HM05737PTDSS1lymphMESH:D001943Breast Neoplasmsbreast
HM05737PTDSS1lymphMESH:D007021Hypospadias
HM05737PTDSS1lymphMESH:D015428Myocardial Reperfusion Injury
HM05737PTDSS1lymphMESH:D019851Thrombophiliabone marrow
HM05737PTDSS1lymphMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05737PTDSS1lymphMESH:D006332Cardiomegaly
HM05737PTDSS1lymphMESH:D009765Obesity
HM05737PTDSS1lymphMESH:D012878Skin Neoplasms
HM05737PTDSS1lymphMESH:D002972Cleft Palate
HM05737PTDSS1lymphMESH:D010382Peliosis Hepatisliver
HM05737PTDSS1lymphMESH:D001169Arthritis, Experimental
HM05737PTDSS1lymphMESH:D017202Myocardial Ischemiaheart
HM05737PTDSS1lymphMESH:D015619Respiratory System Abnormalities
HM05737PTDSS1lymphMESH:D016584Panic Disorder
HM05737PTDSS1lymphMESH:D018248Adenoma, Liver Cell
HM05737PTDSS1lymphMESH:D006973Hypertensionlung
HM05737PTDSS1lymphMESH:D006973Hypertensionheart
HM05737PTDSS1lymphMESH:D006973Hypertensionblood vessel
HM05737PTDSS1lymphMESH:D056486Drug-Induced Liver Injury
HM05737PTDSS1lymphMESH:D002277Carcinoma
HM05737PTDSS1lymphMESH:D011537Pruritus
HM05737PTDSS1lymphMESH:D009369Neoplasmsspleen
HM05737PTDSS1lymphMESH:D009369Neoplasmsbone marrow
HM05737PTDSS1lymphMESH:D017119Porphyria Cutanea Tardaskin
HM05737PTDSS1lymphMESH:D055371Acute Lung Injury
HM05737PTDSS1lymphMESH:D020246Venous Thrombosis
HM05737PTDSS1lymphMESH:D004362Drug Toxicity
HM05737PTDSS1lymphMESH:D008106Liver Cirrhosis, Experimental
HM05737PTDSS1lymphMESH:D001836Body Weight Changes
HM05737PTDSS1lymphMESH:D018281Cholangiocarcinomaliver
HM05737PTDSS1lymphMESH:D006333Heart Failureheart
HM05737PTDSS1lymphMESH:D007249Inflammation
HM05737PTDSS1lymphMESH:D000740Anemiabone marrow
HM05737PTDSS1lymphMESH:D001848Bone Diseases, Developmental
HM05737PTDSS1lymphMESH:D015427Reperfusion Injury
HM05737PTDSS1lymphMESH:D005124Eye Abnormalities
HM05737PTDSS1lymphMESH:D000152Acne Vulgaris
HM05737PTDSS1lymphMESH:D009203Myocardial Infarctionheart
HM05737PTDSS1lymphMESH:D019465Craniofacial Abnormalities
HM05737PTDSS1lymphMESH:D008114Liver Neoplasms, Experimental
HM05737PTDSS1lymphMESH:D013088Spermatocele
HM05737PTDSS1lymphMESH:D013959Thyroid Diseasesthyroid
HM05737PTDSS1lymphMESH:D003876Dermatitis, Atopicskin
HM05737PTDSS1lymphMESH:D006470Hemorrhage
HM05737PTDSS1lymphMESH:D014594Uterine Neoplasmscervix
HM05737PTDSS1lymphMESH:D014594Uterine Neoplasms
HM05737PTDSS1lymphMESH:D005234Fatty Liver
HM05737PTDSS1lymphMESH:D013927Thrombosis
HM05737PTDSS1lymphMESH:D006943Hyperglycemia
HM05737PTDSS1lymphMESH:D001161Arteriosclerosisblood vessel
HM05737PTDSS1lymphMESH:D011297Prenatal Exposure Delayed Effects
HM05737PTDSS1lymphMESH:D006529Hepatomegaly
HM05737PTDSS1lymphMESH:D006869Hydronephrosiskidney
HM05737PTDSS1lymphMESH:D000230Adenocarcinoma
HM05737PTDSS1lymphMESH:D000230Adenocarcinomauterus
HM05737PTDSS1lymphMESH:D000230Adenocarcinoma
HM05737PTDSS1lymphMESH:D000230Adenocarcinoma
HM05737PTDSS1lymphMESH:D000230Adenocarcinomauterus
HM05737PTDSS1lymphMESH:D000230Adenocarcinomathyroid
HM05737PTDSS1lymphMESH:D000230Adenocarcinomaskin
HM05737PTDSS1lymphMESH:D000230Adenocarcinomaparathyroid gland
HM05737PTDSS1lymphMESH:D000230Adenocarcinomaliver
HM05737PTDSS1lymphMESH:D000230Adenocarcinomakidney
HM05737PTDSS1lymphMESH:D000230Adenocarcinomaeye
HM05737PTDSS1lymphMESH:D000230Adenocarcinomaadrenal gland
HM05737PTDSS1lymphMESH:D054079Vascular Malformations
HM05737PTDSS1lymphMESH:D009135Muscular Diseasesmuscle
HM05737PTDSS1lymphMESH:D006330Heart Defects, Congenital
HM05737PTDSS1lymphMESH:D005313Fetal Death
HM05737PTDSS1lymphMESH:D008175Lung Neoplasmslung
HM05737PTDSS1lymphMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM05737PTDSS1lymphMESH:D004487Edema
HM05737PTDSS1lymphMESH:D007247Infertility, Female
HM05737PTDSS1lymphMESH:D019282Wasting Syndrome
HM05737PTDSS1lymphMESH:D000013Congenital Abnormalities
HM05737PTDSS1lymphMESH:D000014Abnormalities, Drug-Induced
HM05737PTDSS1lymphMESH:D001778Blood Coagulation Disordersbone marrow
HM05737PTDSS1lymphMESH:D007569Jaw Abnormalities
HM05737PTDSS1lymphMESH:D005355Fibrosis
HM05737PTDSS1lymphMESH:D009421Nervous System Malformations