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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05123CHMP7lymphMESH:D008114Liver Neoplasms, Experimental
HM05123CHMP7lymphMESH:D013959Thyroid Diseasesthyroid
HM05123CHMP7lymphMESH:D008175Lung Neoplasmslung
HM05123CHMP7lymphMESH:D007569Jaw Abnormalities
HM05123CHMP7lymphMESH:D002972Cleft Palate
HM05123CHMP7lymphMESH:D006332Cardiomegaly
HM05123CHMP7lymphMESH:D005355Fibrosis
HM05123CHMP7lymphMESH:D010382Peliosis Hepatisliver
HM05123CHMP7lymphMESH:D001943Breast Neoplasmsbreast
HM05123CHMP7lymphMESH:D008106Liver Cirrhosis, Experimental
HM05123CHMP7lymphMESH:D004487Edema
HM05123CHMP7lymphMESH:D004489Edema, Cardiac
HM05123CHMP7lymphMESH:D009421Nervous System Malformations
HM05123CHMP7lymphMESH:D017119Porphyria Cutanea Tardaskin
HM05123CHMP7lymphMESH:D015619Respiratory System Abnormalities
HM05123CHMP7lymphMESH:D008113Liver Neoplasms
HM05123CHMP7lymphMESH:D008113Liver Neoplasms
HM05123CHMP7lymphMESH:D019282Wasting Syndrome
HM05123CHMP7lymphMESH:D006973Hypertensionlung
HM05123CHMP7lymphMESH:D006973Hypertensionheart
HM05123CHMP7lymphMESH:D006973Hypertensionblood vessel
HM05123CHMP7lymphMESH:D001848Bone Diseases, Developmental
HM05123CHMP7lymphMESH:D001836Body Weight Changes
HM05123CHMP7lymphMESH:D005124Eye Abnormalities
HM05123CHMP7lymphMESH:D006330Heart Defects, Congenital
HM05123CHMP7lymphMESH:D006470Hemorrhage
HM05123CHMP7lymphMESH:D018281Cholangiocarcinomaliver
HM05123CHMP7lymphMESH:D004362Drug Toxicity
HM05123CHMP7lymphMESH:D011297Prenatal Exposure Delayed Effects
HM05123CHMP7lymphMESH:D006529Hepatomegaly
HM05123CHMP7lymphMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05123CHMP7lymphMESH:D056486Drug-Induced Liver Injury
HM05123CHMP7lymphMESH:D000014Abnormalities, Drug-Induced
HM05123CHMP7lymphMESH:D007249Inflammation
HM05123CHMP7lymphMESH:D002277Carcinoma
HM05123CHMP7lymphMESH:D012878Skin Neoplasms
HM05123CHMP7lymphMESH:D005313Fetal Death
HM05123CHMP7lymphMESH:D018248Adenoma, Liver Cell
HM05123CHMP7lymphMESH:D001778Blood Coagulation Disordersbone marrow
HM05123CHMP7lymphMESH:D000013Congenital Abnormalities
HM05123CHMP7lymphMESH:D017202Myocardial Ischemiaheart
HM05123CHMP7lymphMESH:D019465Craniofacial Abnormalities
HM05123CHMP7lymphMESH:D006869Hydronephrosiskidney
HM05123CHMP7lymphMESH:D054079Vascular Malformations
HM05123CHMP7lymphMESH:D000740Anemiabone marrow