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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03948EMILIN3heartMESH:D006869Hydronephrosiskidney
HM03948EMILIN3heartMESH:D007249Inflammation
HM03948EMILIN3heartMESH:D003920Diabetes Mellituspancreas
HM03948EMILIN3heartMESH:D002972Cleft Palate
HM03948EMILIN3heartMESH:D014605Uveitiseye
HM03948EMILIN3heartMESH:D010382Peliosis Hepatisliver
HM03948EMILIN3heartMESH:D005124Eye Abnormalities
HM03948EMILIN3heartMESH:D005313Fetal Death
HM03948EMILIN3heartMESH:D005355Fibrosis
HM03948EMILIN3heartMESH:D054079Vascular Malformations
HM03948EMILIN3heartMESH:D003924Diabetes Mellitus, Type 2pancreas
HM03948EMILIN3heartMESH:D011297Prenatal Exposure Delayed Effects
HM03948EMILIN3heartMESH:D008113Liver Neoplasms
HM03948EMILIN3heartMESH:D008113Liver Neoplasms
HM03948EMILIN3heartMESH:D017119Porphyria Cutanea Tardaskin
HM03948EMILIN3heartMESH:D006529Hepatomegaly
HM03948EMILIN3heartMESH:D007333Insulin Resistance
HM03948EMILIN3heartMESH:D018248Adenoma, Liver Cell
HM03948EMILIN3heartMESH:D014985Xerophthalmiaeye
HM03948EMILIN3heartMESH:D019465Craniofacial Abnormalities
HM03948EMILIN3heartMESH:D006332Cardiomegaly
HM03948EMILIN3heartMESH:D015619Respiratory System Abnormalities
HM03948EMILIN3heartMESH:D008664Metal Metabolism, Inborn Errorsskin
HM03948EMILIN3heartMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM03948EMILIN3heartMESH:D008664Metal Metabolism, Inborn Errorsliver
HM03948EMILIN3heartMESH:D008664Metal Metabolism, Inborn Errorskidney
HM03948EMILIN3heartMESH:D005885Gingival Hyperplasia
HM03948EMILIN3heartMESH:D001778Blood Coagulation Disordersbone marrow
HM03948EMILIN3heartMESH:D007638Keratoconjunctivitis Siccaeye
HM03948EMILIN3heartMESH:D009404Nephrotic Syndromekidney
HM03948EMILIN3heartMESH:D004487Edema
HM03948EMILIN3heartMESH:D006457Hemoglobinuria, Paroxysmal
HM03948EMILIN3heartMESH:D006470Hemorrhage
HM03948EMILIN3heartMESH:D019457Chromosome Breakage
HM03948EMILIN3heartMESH:D006330Heart Defects, Congenital
HM03948EMILIN3heartMESH:D009402Nephrosis, Lipoidkidney
HM03948EMILIN3heartMESH:D011471Prostatic Neoplasmsprostate
HM03948EMILIN3heartMESH:D008106Liver Cirrhosis, Experimental
HM03948EMILIN3heartMESH:D018281Cholangiocarcinomaliver
HM03948EMILIN3heartMESH:D007674Kidney Diseasesureter
HM03948EMILIN3heartMESH:D007674Kidney Diseasespituitary
HM03948EMILIN3heartMESH:D007674Kidney Diseaseskidney
HM03948EMILIN3heartMESH:D012878Skin Neoplasms
HM03948EMILIN3heartMESH:D001848Bone Diseases, Developmental
HM03948EMILIN3heartMESH:D011565Psoriasisskin
HM03948EMILIN3heartMESH:D000014Abnormalities, Drug-Induced
HM03948EMILIN3heartMESH:D013959Thyroid Diseasesthyroid
HM03948EMILIN3heartMESH:D016393Lymphoma, B-Cell
HM03948EMILIN3heartMESH:D000740Anemiabone marrow
HM03948EMILIN3heartMESH:D008175Lung Neoplasmslung
HM03948EMILIN3heartMESH:D056486Drug-Induced Liver Injury
HM03948EMILIN3heartMESH:D001836Body Weight Changes
HM03948EMILIN3heartMESH:D001943Breast Neoplasmsbreast
HM03948EMILIN3heartMESH:D004362Drug Toxicity
HM03948EMILIN3heartMESH:D002277Carcinoma
HM03948EMILIN3heartMESH:D009421Nervous System Malformations
HM03948EMILIN3heartMESH:D008114Liver Neoplasms, Experimental
HM03948EMILIN3heartMESH:D000013Congenital Abnormalities
HM03948EMILIN3heartMESH:D004489Edema, Cardiac
HM03948EMILIN3heartMESH:D006973Hypertensionlung
HM03948EMILIN3heartMESH:D006973Hypertensionheart
HM03948EMILIN3heartMESH:D006973Hypertensionblood vessel
HM03948EMILIN3heartMESH:D019282Wasting Syndrome
HM03948EMILIN3heartMESH:D007569Jaw Abnormalities
HM03948EMILIN3heartMESH:D017202Myocardial Ischemiaheart