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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04625B3GNT5tracheaMESH:D054079Vascular Malformations
HM04625B3GNT5tracheaMESH:D006869Hydronephrosiskidney
HM04625B3GNT5tracheaMESH:D004362Drug Toxicity
HM04625B3GNT5tracheaMESH:D017202Myocardial Ischemiaheart
HM04625B3GNT5tracheaMESH:D014985Xerophthalmiaeye
HM04625B3GNT5tracheaMESH:D009404Nephrotic Syndromekidney
HM04625B3GNT5tracheaMESH:D007569Jaw Abnormalities
HM04625B3GNT5tracheaMESH:D001943Breast Neoplasmsbreast
HM04625B3GNT5tracheaMESH:D014605Uveitiseye
HM04625B3GNT5tracheaMESH:D010995Pleural Diseasesbone
HM04625B3GNT5tracheaMESH:D006470Hemorrhage
HM04625B3GNT5tracheaMESH:D007638Keratoconjunctivitis Siccaeye
HM04625B3GNT5tracheaMESH:D008113Liver Neoplasms
HM04625B3GNT5tracheaMESH:D008113Liver Neoplasms
HM04625B3GNT5tracheaMESH:D006973Hypertensionlung
HM04625B3GNT5tracheaMESH:D006973Hypertensionheart
HM04625B3GNT5tracheaMESH:D006973Hypertensionblood vessel
HM04625B3GNT5tracheaMESH:D005124Eye Abnormalities
HM04625B3GNT5tracheaMESH:D011658Pulmonary Fibrosislung
HM04625B3GNT5tracheaMESH:D019465Craniofacial Abnormalities
HM04625B3GNT5tracheaMESH:D005313Fetal Death
HM04625B3GNT5tracheaMESH:D011297Prenatal Exposure Delayed Effects
HM04625B3GNT5tracheaMESH:D009421Nervous System Malformations
HM04625B3GNT5tracheaMESH:D011565Psoriasisskin
HM04625B3GNT5tracheaMESH:D056486Drug-Induced Liver Injury
HM04625B3GNT5tracheaMESH:D008114Liver Neoplasms, Experimental
HM04625B3GNT5tracheaMESH:D000014Abnormalities, Drug-Induced
HM04625B3GNT5tracheaMESH:D006330Heart Defects, Congenital
HM04625B3GNT5tracheaMESH:D055370Lung Injury
HM04625B3GNT5tracheaMESH:D015619Respiratory System Abnormalities
HM04625B3GNT5tracheaMESH:D002277Carcinoma
HM04625B3GNT5tracheaMESH:D018281Cholangiocarcinomaliver
HM04625B3GNT5tracheaMESH:D004489Edema, Cardiac
HM04625B3GNT5tracheaMESH:D008175Lung Neoplasmslung
HM04625B3GNT5tracheaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM04625B3GNT5tracheaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM04625B3GNT5tracheaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM04625B3GNT5tracheaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM04625B3GNT5tracheaMESH:D018248Adenoma, Liver Cell
HM04625B3GNT5tracheaMESH:D006457Hemoglobinuria, Paroxysmal
HM04625B3GNT5tracheaMESH:D017119Porphyria Cutanea Tardaskin
HM04625B3GNT5tracheaMESH:D008654Mesotheliomabone
HM04625B3GNT5tracheaMESH:D005355Fibrosis
HM04625B3GNT5tracheaMESH:D006529Hepatomegaly
HM04625B3GNT5tracheaMESH:D007674Kidney Diseasesureter
HM04625B3GNT5tracheaMESH:D007674Kidney Diseasespituitary
HM04625B3GNT5tracheaMESH:D007674Kidney Diseaseskidney
HM04625B3GNT5tracheaMESH:D008106Liver Cirrhosis, Experimental
HM04625B3GNT5tracheaMESH:D010382Peliosis Hepatisliver
HM04625B3GNT5tracheaMESH:D001778Blood Coagulation Disordersbone marrow
HM04625B3GNT5tracheaMESH:D001836Body Weight Changes
HM04625B3GNT5tracheaMESH:D006332Cardiomegaly
HM04625B3GNT5tracheaMESH:D002972Cleft Palate
HM04625B3GNT5tracheaMESH:D006528Carcinoma, Hepatocellularliver
HM04625B3GNT5tracheaMESH:D000013Congenital Abnormalities
HM04625B3GNT5tracheaMESH:D009402Nephrosis, Lipoidkidney
HM04625B3GNT5tracheaMESH:D011471Prostatic Neoplasmsprostate
HM04625B3GNT5tracheaMESH:D001848Bone Diseases, Developmental
HM04625B3GNT5tracheaMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04625B3GNT5tracheaMESH:D005885Gingival Hyperplasia
HM04625B3GNT5tracheaMESH:D012878Skin Neoplasms
HM04625B3GNT5tracheaMESH:D019282Wasting Syndrome
HM04625B3GNT5tracheaMESH:D004487Edema
HM04625B3GNT5tracheaMESH:D007249Inflammation
HM04625B3GNT5tracheaMESH:D000740Anemiabone marrow
HM04625B3GNT5tracheaMESH:D013959Thyroid Diseasesthyroid