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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04027RHOJamnionMESH:D008325Mammary Neoplasms, Experimental
HM04027RHOJamnionMESH:D005124Eye Abnormalities
HM04027RHOJamnionMESH:D007248Infertility, Male
HM04027RHOJamnionMESH:D019636Neurodegenerative Diseasesnerve
HM04027RHOJamnionMESH:D015619Respiratory System Abnormalities
HM04027RHOJamnionMESH:D030342Genetic Diseases, Inborn
HM04027RHOJamnionMESH:D008546Melanoma, Experimental
HM04027RHOJamnionMESH:D019282Wasting Syndrome
HM04027RHOJamnionMESH:D001321Autistic Disorder
HM04027RHOJamnionMESH:D017114Liver Failure, Acute
HM04027RHOJamnionMESH:D008113Liver Neoplasms
HM04027RHOJamnionMESH:D008113Liver Neoplasms
HM04027RHOJamnionMESH:D008175Lung Neoplasmslung
HM04027RHOJamnionMESH:D018281Cholangiocarcinomaliver
HM04027RHOJamnionMESH:D000013Congenital Abnormalities
HM04027RHOJamnionMESH:D006973Hypertensionlung
HM04027RHOJamnionMESH:D006973Hypertensionheart
HM04027RHOJamnionMESH:D006973Hypertensionblood vessel
HM04027RHOJamnionMESH:D010146Pain
HM04027RHOJamnionMESH:D019465Craniofacial Abnormalities
HM04027RHOJamnionMESH:D001943Breast Neoplasmsbreast
HM04027RHOJamnionMESH:D017119Porphyria Cutanea Tardaskin
HM04027RHOJamnionMESH:D018248Adenoma, Liver Cell
HM04027RHOJamnionMESH:D014581Urticariaskin
HM04027RHOJamnionMESH:D005313Fetal Death
HM04027RHOJamnionMESH:D010382Peliosis Hepatisliver
HM04027RHOJamnionMESH:D004487Edema
HM04027RHOJamnionMESH:D003456Cryptorchidism
HM04027RHOJamnionMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM04027RHOJamnionMESH:D007249Inflammation
HM04027RHOJamnionMESH:D017202Myocardial Ischemiaheart
HM04027RHOJamnionMESH:D001848Bone Diseases, Developmental
HM04027RHOJamnionMESH:D006470Hemorrhage
HM04027RHOJamnionMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04027RHOJamnionMESH:D008106Liver Cirrhosis, Experimental
HM04027RHOJamnionMESH:D000799Angioedemaskin
HM04027RHOJamnionMESH:D007674Kidney Diseasesureter
HM04027RHOJamnionMESH:D007674Kidney Diseasespituitary
HM04027RHOJamnionMESH:D007674Kidney Diseaseskidney
HM04027RHOJamnionMESH:D056486Drug-Induced Liver Injury
HM04027RHOJamnionMESH:D009421Nervous System Malformations
HM04027RHOJamnionMESH:D001008Anxiety Disorders
HM04027RHOJamnionMESH:D006529Hepatomegaly
HM04027RHOJamnionMESH:D006930Hyperalgesia
HM04027RHOJamnionMESH:D007984Leydig Cell Tumor
HM04027RHOJamnionMESH:D002972Cleft Palate
HM04027RHOJamnionMESH:D007569Jaw Abnormalities
HM04027RHOJamnionMESH:D011297Prenatal Exposure Delayed Effects
HM04027RHOJamnionMESH:D005832Genital Diseases, Maletestis
HM04027RHOJamnionMESH:D005832Genital Diseases, Maleprostate
HM04027RHOJamnionMESH:D005832Genital Diseases, Maleblood vessel
HM04027RHOJamnionMESH:D006330Heart Defects, Congenital
HM04027RHOJamnionMESH:D011472Prostatitisprostate
HM04027RHOJamnionMESH:D013959Thyroid Diseasesthyroid
HM04027RHOJamnionMESH:D002277Carcinoma
HM04027RHOJamnionMESH:D004362Drug Toxicity
HM04027RHOJamnionMESH:D005355Fibrosis
HM04027RHOJamnionMESH:D006869Hydronephrosiskidney
HM04027RHOJamnionMESH:D054079Vascular Malformations
HM04027RHOJamnionMESH:D000014Abnormalities, Drug-Induced
HM04027RHOJamnionMESH:D008114Liver Neoplasms, Experimental
HM04027RHOJamnionMESH:D004489Edema, Cardiac
HM04027RHOJamnionMESH:D000740Anemiabone marrow
HM04027RHOJamnionMESH:D011469Prostatic Diseasesureter
HM04027RHOJamnionMESH:D011469Prostatic Diseasesprostate
HM04027RHOJamnionMESH:D012878Skin Neoplasms
HM04027RHOJamnionMESH:D006332Cardiomegaly
HM04027RHOJamnionMESH:D003921Diabetes Mellitus, Experimental
HM04027RHOJamnionMESH:D008107Liver Diseasesskin
HM04027RHOJamnionMESH:D008107Liver Diseasesmuscle
HM04027RHOJamnionMESH:D008107Liver Diseaseslung
HM04027RHOJamnionMESH:D008107Liver Diseasesliver
HM04027RHOJamnionMESH:D001778Blood Coagulation Disordersbone marrow
HM04027RHOJamnionMESH:D001836Body Weight Changes
HM04027RHOJamnionMESH:D002386Cataractpancreas
HM04027RHOJamnionMESH:D002386Cataracteye