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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04296EVPLthyroidMESH:D011014Pneumonialung
HM04296EVPLthyroidMESH:D019966Substance-Related Disorders
HM04296EVPLthyroidMESH:D004489Edema, Cardiac
HM04296EVPLthyroidMESH:D012878Skin Neoplasms
HM04296EVPLthyroidMESH:D014591Uterine Diseasesuterus
HM04296EVPLthyroidMESH:D014591Uterine Diseasesplacenta
HM04296EVPLthyroidMESH:D014591Uterine Diseasescervix
HM04296EVPLthyroidMESH:D008325Mammary Neoplasms, Experimental
HM04296EVPLthyroidMESH:D013959Thyroid Diseasesthyroid
HM04296EVPLthyroidMESH:D054079Vascular Malformations
HM04296EVPLthyroidMESH:D002972Cleft Palate
HM04296EVPLthyroidMESH:D015619Respiratory System Abnormalities
HM04296EVPLthyroidMESH:D002277Carcinoma
HM04296EVPLthyroidMESH:D006470Hemorrhage
HM04296EVPLthyroidMESH:D006869Hydronephrosiskidney
HM04296EVPLthyroidMESH:D008113Liver Neoplasms
HM04296EVPLthyroidMESH:D008113Liver Neoplasms
HM04296EVPLthyroidMESH:D018248Adenoma, Liver Cell
HM04296EVPLthyroidMESH:D008114Liver Neoplasms, Experimental
HM04296EVPLthyroidMESH:D006529Hepatomegaly
HM04296EVPLthyroidMESH:D005313Fetal Death
HM04296EVPLthyroidMESH:D007333Insulin Resistance
HM04296EVPLthyroidMESH:D009421Nervous System Malformations
HM04296EVPLthyroidMESH:D001862Bone Resorption
HM04296EVPLthyroidMESH:D008106Liver Cirrhosis, Experimental
HM04296EVPLthyroidMESH:D001778Blood Coagulation Disordersbone marrow
HM04296EVPLthyroidMESH:D000013Congenital Abnormalities
HM04296EVPLthyroidMESH:D006332Cardiomegaly
HM04296EVPLthyroidMESH:D019282Wasting Syndrome
HM04296EVPLthyroidMESH:D056486Drug-Induced Liver Injury
HM04296EVPLthyroidMESH:D005124Eye Abnormalities
HM04296EVPLthyroidMESH:D006967Hypersensitivitybone marrow
HM04296EVPLthyroidMESH:D007249Inflammation
HM04296EVPLthyroidMESH:D010049Ovarian Diseasesovary
HM04296EVPLthyroidMESH:D011297Prenatal Exposure Delayed Effects
HM04296EVPLthyroidMESH:D001848Bone Diseases, Developmental
HM04296EVPLthyroidMESH:D004487Edema
HM04296EVPLthyroidMESH:D017119Porphyria Cutanea Tardaskin
HM04296EVPLthyroidMESH:D006330Heart Defects, Congenital
HM04296EVPLthyroidMESH:D019465Craniofacial Abnormalities
HM04296EVPLthyroidMESH:D001943Breast Neoplasmsbreast
HM04296EVPLthyroidMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04296EVPLthyroidMESH:D002278Carcinoma in Situ
HM04296EVPLthyroidMESH:D002278Carcinoma in Situ
HM04296EVPLthyroidMESH:D011629Puberty, Precocious
HM04296EVPLthyroidMESH:D000740Anemiabone marrow
HM04296EVPLthyroidMESH:D018281Cholangiocarcinomaliver
HM04296EVPLthyroidMESH:D001836Body Weight Changes
HM04296EVPLthyroidMESH:D008175Lung Neoplasmslung
HM04296EVPLthyroidMESH:D006973Hypertensionlung
HM04296EVPLthyroidMESH:D006973Hypertensionheart
HM04296EVPLthyroidMESH:D006973Hypertensionblood vessel
HM04296EVPLthyroidMESH:D000014Abnormalities, Drug-Induced
HM04296EVPLthyroidMESH:D010382Peliosis Hepatisliver
HM04296EVPLthyroidMESH:D004362Drug Toxicity
HM04296EVPLthyroidMESH:D005355Fibrosis
HM04296EVPLthyroidMESH:D011471Prostatic Neoplasmsprostate
HM04296EVPLthyroidMESH:D007569Jaw Abnormalities
HM04296EVPLthyroidMESH:D017202Myocardial Ischemiaheart