Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04849CDH12blood vesselMESH:D000013Congenital Abnormalities
HM04849CDH12blood vesselMESH:D019465Craniofacial Abnormalities
HM04849CDH12blood vesselMESH:D009402Nephrosis, Lipoidkidney
HM04849CDH12blood vesselMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04849CDH12blood vesselMESH:D002972Cleft Palate
HM04849CDH12blood vesselMESH:D008175Lung Neoplasmslung
HM04849CDH12blood vesselMESH:D017119Porphyria Cutanea Tardaskin
HM04849CDH12blood vesselMESH:D007638Keratoconjunctivitis Siccaeye
HM04849CDH12blood vesselMESH:D005355Fibrosis
HM04849CDH12blood vesselMESH:D011565Psoriasisskin
HM04849CDH12blood vesselMESH:D008106Liver Cirrhosis, Experimental
HM04849CDH12blood vesselMESH:D017202Myocardial Ischemiaheart
HM04849CDH12blood vesselMESH:D006973Hypertensionlung
HM04849CDH12blood vesselMESH:D006973Hypertensionheart
HM04849CDH12blood vesselMESH:D006973Hypertensionblood vessel
HM04849CDH12blood vesselMESH:D004487Edema
HM04849CDH12blood vesselMESH:D006529Hepatomegaly
HM04849CDH12blood vesselMESH:D002277Carcinoma
HM04849CDH12blood vesselMESH:D000740Anemiabone marrow
HM04849CDH12blood vesselMESH:D000014Abnormalities, Drug-Induced
HM04849CDH12blood vesselMESH:D014985Xerophthalmiaeye
HM04849CDH12blood vesselMESH:D006869Hydronephrosiskidney
HM04849CDH12blood vesselMESH:D008113Liver Neoplasms
HM04849CDH12blood vesselMESH:D008113Liver Neoplasms
HM04849CDH12blood vesselMESH:D008664Metal Metabolism, Inborn Errorsskin
HM04849CDH12blood vesselMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM04849CDH12blood vesselMESH:D008664Metal Metabolism, Inborn Errorsliver
HM04849CDH12blood vesselMESH:D008664Metal Metabolism, Inborn Errorskidney
HM04849CDH12blood vesselMESH:D013959Thyroid Diseasesthyroid
HM04849CDH12blood vesselMESH:D056486Drug-Induced Liver Injury
HM04849CDH12blood vesselMESH:D014605Uveitiseye
HM04849CDH12blood vesselMESH:D007569Jaw Abnormalities
HM04849CDH12blood vesselMESH:D007249Inflammation
HM04849CDH12blood vesselMESH:D001848Bone Diseases, Developmental
HM04849CDH12blood vesselMESH:D006528Carcinoma, Hepatocellularliver
HM04849CDH12blood vesselMESH:D007674Kidney Diseasesureter
HM04849CDH12blood vesselMESH:D007674Kidney Diseasespituitary
HM04849CDH12blood vesselMESH:D007674Kidney Diseaseskidney
HM04849CDH12blood vesselMESH:D005313Fetal Death
HM04849CDH12blood vesselMESH:D008114Liver Neoplasms, Experimental
HM04849CDH12blood vesselMESH:D004489Edema, Cardiac
HM04849CDH12blood vesselMESH:D018281Cholangiocarcinomaliver
HM04849CDH12blood vesselMESH:D054079Vascular Malformations
HM04849CDH12blood vesselMESH:D009404Nephrotic Syndromekidney
HM04849CDH12blood vesselMESH:D009421Nervous System Malformations
HM04849CDH12blood vesselMESH:D001778Blood Coagulation Disordersbone marrow
HM04849CDH12blood vesselMESH:D005124Eye Abnormalities
HM04849CDH12blood vesselMESH:D006330Heart Defects, Congenital
HM04849CDH12blood vesselMESH:D018248Adenoma, Liver Cell
HM04849CDH12blood vesselMESH:D004362Drug Toxicity
HM04849CDH12blood vesselMESH:D005885Gingival Hyperplasia
HM04849CDH12blood vesselMESH:D012878Skin Neoplasms
HM04849CDH12blood vesselMESH:D010382Peliosis Hepatisliver
HM04849CDH12blood vesselMESH:D006332Cardiomegaly
HM04849CDH12blood vesselMESH:D006457Hemoglobinuria, Paroxysmal
HM04849CDH12blood vesselMESH:D011297Prenatal Exposure Delayed Effects
HM04849CDH12blood vesselMESH:D015619Respiratory System Abnormalities
HM04849CDH12blood vesselMESH:D001943Breast Neoplasmsbreast
HM04849CDH12blood vesselMESH:D006470Hemorrhage
HM04849CDH12blood vesselMESH:D019282Wasting Syndrome
HM04849CDH12blood vesselMESH:D001836Body Weight Changes