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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01958KRT37colonMESH:D007249Inflammation
HM01958KRT37colonMESH:D018281Cholangiocarcinomaliver
HM01958KRT37colonMESH:D019282Wasting Syndrome
HM01958KRT37colonMESH:D004362Drug Toxicity
HM01958KRT37colonMESH:D002277Carcinoma
HM01958KRT37colonMESH:D054079Vascular Malformations
HM01958KRT37colonMESH:D009421Nervous System Malformations
HM01958KRT37colonMESH:D000014Abnormalities, Drug-Induced
HM01958KRT37colonMESH:D012878Skin Neoplasms
HM01958KRT37colonMESH:D056486Drug-Induced Liver Injury
HM01958KRT37colonMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01958KRT37colonMESH:D010382Peliosis Hepatisliver
HM01958KRT37colonMESH:D017119Porphyria Cutanea Tardaskin
HM01958KRT37colonMESH:D006330Heart Defects, Congenital
HM01958KRT37colonMESH:D019465Craniofacial Abnormalities
HM01958KRT37colonMESH:D013959Thyroid Diseasesthyroid
HM01958KRT37colonMESH:D001836Body Weight Changes
HM01958KRT37colonMESH:D004487Edema
HM01958KRT37colonMESH:D011471Prostatic Neoplasmsprostate
HM01958KRT37colonMESH:D011297Prenatal Exposure Delayed Effects
HM01958KRT37colonMESH:D000740Anemiabone marrow
HM01958KRT37colonMESH:D001848Bone Diseases, Developmental
HM01958KRT37colonMESH:D005313Fetal Death
HM01958KRT37colonMESH:D011470Prostatic Hyperplasia
HM01958KRT37colonMESH:D001943Breast Neoplasmsbreast
HM01958KRT37colonMESH:D004489Edema, Cardiac
HM01958KRT37colonMESH:D006973Hypertensionlung
HM01958KRT37colonMESH:D006973Hypertensionheart
HM01958KRT37colonMESH:D006973Hypertensionblood vessel
HM01958KRT37colonMESH:D002294Carcinoma, Squamous Celllung
HM01958KRT37colonMESH:D002294Carcinoma, Squamous Cellliver
HM01958KRT37colonMESH:D002294Carcinoma, Squamous Celllarynx
HM01958KRT37colonMESH:D002294Carcinoma, Squamous Cellkidney
HM01958KRT37colonMESH:D002294Carcinoma, Squamous Celleye
HM01958KRT37colonMESH:D006529Hepatomegaly
HM01958KRT37colonMESH:D017202Myocardial Ischemiaheart
HM01958KRT37colonMESH:D005355Fibrosis
HM01958KRT37colonMESH:D007569Jaw Abnormalities
HM01958KRT37colonMESH:D015619Respiratory System Abnormalities
HM01958KRT37colonMESH:D002972Cleft Palate
HM01958KRT37colonMESH:D001778Blood Coagulation Disordersbone marrow
HM01958KRT37colonMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM01958KRT37colonMESH:D005124Eye Abnormalities
HM01958KRT37colonMESH:D008106Liver Cirrhosis, Experimental
HM01958KRT37colonMESH:D008175Lung Neoplasmslung
HM01958KRT37colonMESH:D000013Congenital Abnormalities
HM01958KRT37colonMESH:D006332Cardiomegaly
HM01958KRT37colonMESH:D006470Hemorrhage
HM01958KRT37colonMESH:D018248Adenoma, Liver Cell
HM01958KRT37colonMESH:D006869Hydronephrosiskidney
HM01958KRT37colonMESH:D008113Liver Neoplasms
HM01958KRT37colonMESH:D008113Liver Neoplasms
HM01958KRT37colonMESH:D008114Liver Neoplasms, Experimental