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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00696VNN2bloodMESH:D010382Peliosis Hepatisliver
HM00696VNN2bloodMESH:D001836Body Weight Changes
HM00696VNN2bloodMESH:D017202Myocardial Ischemiaheart
HM00696VNN2bloodMESH:D006869Hydronephrosiskidney
HM00696VNN2bloodMESH:D013959Thyroid Diseasesthyroid
HM00696VNN2bloodMESH:D006529Hepatomegaly
HM00696VNN2bloodMESH:D008106Liver Cirrhosis, Experimental
HM00696VNN2bloodMESH:D001778Blood Coagulation Disordersbone marrow
HM00696VNN2bloodMESH:D008113Liver Neoplasms
HM00696VNN2bloodMESH:D008113Liver Neoplasms
HM00696VNN2bloodMESH:D004362Drug Toxicity
HM00696VNN2bloodMESH:D000740Anemiabone marrow
HM00696VNN2bloodMESH:D006470Hemorrhage
HM00696VNN2bloodMESH:D008114Liver Neoplasms, Experimental
HM00696VNN2bloodMESH:D008175Lung Neoplasmslung
HM00696VNN2bloodMESH:D000014Abnormalities, Drug-Induced
HM00696VNN2bloodMESH:D001848Bone Diseases, Developmental
HM00696VNN2bloodMESH:D019465Craniofacial Abnormalities
HM00696VNN2bloodMESH:D006973Hypertensionlung
HM00696VNN2bloodMESH:D006973Hypertensionheart
HM00696VNN2bloodMESH:D006973Hypertensionblood vessel
HM00696VNN2bloodMESH:D007569Jaw Abnormalities
HM00696VNN2bloodMESH:D019282Wasting Syndrome
HM00696VNN2bloodMESH:D005313Fetal Death
HM00696VNN2bloodMESH:D018248Adenoma, Liver Cell
HM00696VNN2bloodMESH:D012878Skin Neoplasms
HM00696VNN2bloodMESH:D004487Edema
HM00696VNN2bloodMESH:D004489Edema, Cardiac
HM00696VNN2bloodMESH:D001943Breast Neoplasmsbreast
HM00696VNN2bloodMESH:D017119Porphyria Cutanea Tardaskin
HM00696VNN2bloodMESH:D054079Vascular Malformations
HM00696VNN2bloodMESH:D000013Congenital Abnormalities
HM00696VNN2bloodMESH:D018281Cholangiocarcinomaliver
HM00696VNN2bloodMESH:D002972Cleft Palate
HM00696VNN2bloodMESH:D005124Eye Abnormalities
HM00696VNN2bloodMESH:D005355Fibrosis
HM00696VNN2bloodMESH:D011297Prenatal Exposure Delayed Effects
HM00696VNN2bloodMESH:D056486Drug-Induced Liver Injury
HM00696VNN2bloodMESH:D006330Heart Defects, Congenital
HM00696VNN2bloodMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00696VNN2bloodMESH:D009421Nervous System Malformations
HM00696VNN2bloodMESH:D006332Cardiomegaly
HM00696VNN2bloodMESH:D007249Inflammation
HM00696VNN2bloodMESH:D015619Respiratory System Abnormalities
HM00696VNN2bloodMESH:D002277Carcinoma