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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04693AADATblood vesselMESH:D000740Anemiabone marrow
HM04693AADATblood vesselMESH:D001778Blood Coagulation Disordersbone marrow
HM04693AADATblood vesselMESH:D007674Kidney Diseasesureter
HM04693AADATblood vesselMESH:D007674Kidney Diseasespituitary
HM04693AADATblood vesselMESH:D007674Kidney Diseaseskidney
HM04693AADATblood vesselMESH:D008114Liver Neoplasms, Experimental
HM04693AADATblood vesselMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04693AADATblood vesselMESH:D000799Angioedemaskin
HM04693AADATblood vesselMESH:D019282Wasting Syndrome
HM04693AADATblood vesselMESH:D018248Adenoma, Liver Cell
HM04693AADATblood vesselMESH:D006332Cardiomegaly
HM04693AADATblood vesselMESH:D000014Abnormalities, Drug-Induced
HM04693AADATblood vesselMESH:D008546Melanoma, Experimental
HM04693AADATblood vesselMESH:D002471Cell Transformation, Neoplastic
HM04693AADATblood vesselMESH:D054079Vascular Malformations
HM04693AADATblood vesselMESH:D008175Lung Neoplasmslung
HM04693AADATblood vesselMESH:D006930Hyperalgesia
HM04693AADATblood vesselMESH:D004362Drug Toxicity
HM04693AADATblood vesselMESH:D008107Liver Diseasesskin
HM04693AADATblood vesselMESH:D008107Liver Diseasesmuscle
HM04693AADATblood vesselMESH:D008107Liver Diseaseslung
HM04693AADATblood vesselMESH:D008107Liver Diseasesliver
HM04693AADATblood vesselMESH:D019465Craniofacial Abnormalities
HM04693AADATblood vesselMESH:D008113Liver Neoplasms
HM04693AADATblood vesselMESH:D008113Liver Neoplasms
HM04693AADATblood vesselMESH:D012878Skin Neoplasms
HM04693AADATblood vesselMESH:D000013Congenital Abnormalities
HM04693AADATblood vesselMESH:D010146Pain
HM04693AADATblood vesselMESH:D007569Jaw Abnormalities
HM04693AADATblood vesselMESH:D006973Hypertensionlung
HM04693AADATblood vesselMESH:D006973Hypertensionheart
HM04693AADATblood vesselMESH:D006973Hypertensionblood vessel
HM04693AADATblood vesselMESH:D009421Nervous System Malformations
HM04693AADATblood vesselMESH:D019636Neurodegenerative Diseasesnerve
HM04693AADATblood vesselMESH:D017119Porphyria Cutanea Tardaskin
HM04693AADATblood vesselMESH:D006470Hemorrhage
HM04693AADATblood vesselMESH:D017114Liver Failure, Acute
HM04693AADATblood vesselMESH:D013959Thyroid Diseasesthyroid
HM04693AADATblood vesselMESH:D001848Bone Diseases, Developmental
HM04693AADATblood vesselMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM04693AADATblood vesselMESH:D005313Fetal Death
HM04693AADATblood vesselMESH:D005124Eye Abnormalities
HM04693AADATblood vesselMESH:D056486Drug-Induced Liver Injury
HM04693AADATblood vesselMESH:D001289Attention Deficit Disorder with Hyperactivity
HM04693AADATblood vesselMESH:D005355Fibrosis
HM04693AADATblood vesselMESH:D004938Esophageal Neoplasms
HM04693AADATblood vesselMESH:D011297Prenatal Exposure Delayed Effects
HM04693AADATblood vesselMESH:D001321Autistic Disorder
HM04693AADATblood vesselMESH:D004489Edema, Cardiac
HM04693AADATblood vesselMESH:D001943Breast Neoplasmsbreast
HM04693AADATblood vesselMESH:D002972Cleft Palate
HM04693AADATblood vesselMESH:D006330Heart Defects, Congenital
HM04693AADATblood vesselMESH:D017202Myocardial Ischemiaheart
HM04693AADATblood vesselMESH:D015619Respiratory System Abnormalities
HM04693AADATblood vesselMESH:D008106Liver Cirrhosis, Experimental
HM04693AADATblood vesselMESH:D002277Carcinoma
HM04693AADATblood vesselMESH:D006869Hydronephrosiskidney
HM04693AADATblood vesselMESH:D001836Body Weight Changes
HM04693AADATblood vesselMESH:D002386Cataractpancreas
HM04693AADATblood vesselMESH:D002386Cataracteye
HM04693AADATblood vesselMESH:D018281Cholangiocarcinomaliver
HM04693AADATblood vesselMESH:D010382Peliosis Hepatisliver
HM04693AADATblood vesselMESH:D014581Urticariaskin
HM04693AADATblood vesselMESH:D004487Edema
HM04693AADATblood vesselMESH:D006529Hepatomegaly
HM04693AADATblood vesselMESH:D007249Inflammation