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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01353PSG7placentaMESH:D008175Lung Neoplasmslung
HM01353PSG7placentaMESH:D004487Edema
HM01353PSG7placentaMESH:D013959Thyroid Diseasesthyroid
HM01353PSG7placentaMESH:D019282Wasting Syndrome
HM01353PSG7placentaMESH:D000013Congenital Abnormalities
HM01353PSG7placentaMESH:D008114Liver Neoplasms, Experimental
HM01353PSG7placentaMESH:D002277Carcinoma
HM01353PSG7placentaMESH:D011471Prostatic Neoplasmsprostate
HM01353PSG7placentaMESH:D004938Esophageal Neoplasms
HM01353PSG7placentaMESH:D009421Nervous System Malformations
HM01353PSG7placentaMESH:D005124Eye Abnormalities
HM01353PSG7placentaMESH:D019465Craniofacial Abnormalities
HM01353PSG7placentaMESH:D015619Respiratory System Abnormalities
HM01353PSG7placentaMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01353PSG7placentaMESH:D000740Anemiabone marrow
HM01353PSG7placentaMESH:D002972Cleft Palate
HM01353PSG7placentaMESH:D015179Colorectal Neoplasms
HM01353PSG7placentaMESH:D011297Prenatal Exposure Delayed Effects
HM01353PSG7placentaMESH:D017202Myocardial Ischemiaheart
HM01353PSG7placentaMESH:D010300Parkinson Diseasenerve
HM01353PSG7placentaMESH:D004489Edema, Cardiac
HM01353PSG7placentaMESH:D018281Cholangiocarcinomaliver
HM01353PSG7placentaMESH:D006529Hepatomegaly
HM01353PSG7placentaMESH:D008106Liver Cirrhosis, Experimental
HM01353PSG7placentaMESH:D006330Heart Defects, Congenital
HM01353PSG7placentaMESH:D054079Vascular Malformations
HM01353PSG7placentaMESH:D001848Bone Diseases, Developmental
HM01353PSG7placentaMESH:D006973Hypertensionlung
HM01353PSG7placentaMESH:D006973Hypertensionheart
HM01353PSG7placentaMESH:D006973Hypertensionblood vessel
HM01353PSG7placentaMESH:D001943Breast Neoplasmsbreast
HM01353PSG7placentaMESH:D056486Drug-Induced Liver Injury
HM01353PSG7placentaMESH:D004362Drug Toxicity
HM01353PSG7placentaMESH:D006332Cardiomegaly
HM01353PSG7placentaMESH:D003704Dementianerve
HM01353PSG7placentaMESH:D003704Dementiablood vessel
HM01353PSG7placentaMESH:D007569Jaw Abnormalities
HM01353PSG7placentaMESH:D012878Skin Neoplasms
HM01353PSG7placentaMESH:D005355Fibrosis
HM01353PSG7placentaMESH:D010382Peliosis Hepatisliver
HM01353PSG7placentaMESH:D006470Hemorrhage
HM01353PSG7placentaMESH:D017119Porphyria Cutanea Tardaskin
HM01353PSG7placentaMESH:D018248Adenoma, Liver Cell
HM01353PSG7placentaMESH:D002471Cell Transformation, Neoplastic
HM01353PSG7placentaMESH:D005313Fetal Death
HM01353PSG7placentaMESH:D006869Hydronephrosiskidney
HM01353PSG7placentaMESH:D001778Blood Coagulation Disordersbone marrow
HM01353PSG7placentaMESH:D001836Body Weight Changes
HM01353PSG7placentaMESH:D007249Inflammation
HM01353PSG7placentaMESH:D008113Liver Neoplasms
HM01353PSG7placentaMESH:D008113Liver Neoplasms
HM01353PSG7placentaMESH:D000014Abnormalities, Drug-Induced