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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00797FSTL3placentaMESH:D006973Hypertensionlung
HM00797FSTL3placentaMESH:D006973Hypertensionheart
HM00797FSTL3placentaMESH:D006973Hypertensionblood vessel
HM00797FSTL3placentaMESH:D008114Liver Neoplasms, Experimental
HM00797FSTL3placentaMESH:D008325Mammary Neoplasms, Experimental
HM00797FSTL3placentaMESH:D002277Carcinoma
HM00797FSTL3placentaMESH:D019465Craniofacial Abnormalities
HM00797FSTL3placentaMESH:D006932Hyperbilirubinemia
HM00797FSTL3placentaMESH:D010382Peliosis Hepatisliver
HM00797FSTL3placentaMESH:D013959Thyroid Diseasesthyroid
HM00797FSTL3placentaMESH:D007674Kidney Diseasesureter
HM00797FSTL3placentaMESH:D007674Kidney Diseasespituitary
HM00797FSTL3placentaMESH:D007674Kidney Diseaseskidney
HM00797FSTL3placentaMESH:D008175Lung Neoplasmslung
HM00797FSTL3placentaMESH:D001145Arrhythmias, Cardiac
HM00797FSTL3placentaMESH:D005234Fatty Liver
HM00797FSTL3placentaMESH:D015619Respiratory System Abnormalities
HM00797FSTL3placentaMESH:D004715Endometriosisuterus
HM00797FSTL3placentaMESH:D004715Endometriosisovary
HM00797FSTL3placentaMESH:D011297Prenatal Exposure Delayed Effects
HM00797FSTL3placentaMESH:D001943Breast Neoplasmsbreast
HM00797FSTL3placentaMESH:D001848Bone Diseases, Developmental
HM00797FSTL3placentaMESH:D002252Carbon Tetrachloride Poisoning
HM00797FSTL3placentaMESH:D006984Hypertrophy
HM00797FSTL3placentaMESH:D004362Drug Toxicity
HM00797FSTL3placentaMESH:D006332Cardiomegaly
HM00797FSTL3placentaMESH:D005885Gingival Hyperplasia
HM00797FSTL3placentaMESH:D007638Keratoconjunctivitis Siccaeye
HM00797FSTL3placentaMESH:D012135Respiratory Sounds
HM00797FSTL3placentaMESH:D014985Xerophthalmiaeye
HM00797FSTL3placentaMESH:D000382Agricultural Workers' Diseases
HM00797FSTL3placentaMESH:D007248Infertility, Male
HM00797FSTL3placentaMESH:D008113Liver Neoplasms
HM00797FSTL3placentaMESH:D008113Liver Neoplasms
HM00797FSTL3placentaMESH:D017202Myocardial Ischemiaheart
HM00797FSTL3placentaMESH:D006529Hepatomegaly
HM00797FSTL3placentaMESH:D010051Ovarian Neoplasmsuterus
HM00797FSTL3placentaMESH:D010051Ovarian Neoplasms
HM00797FSTL3placentaMESH:D001919Bradycardia
HM00797FSTL3placentaMESH:D004489Edema, Cardiac
HM00797FSTL3placentaMESH:D008107Liver Diseasesskin
HM00797FSTL3placentaMESH:D008107Liver Diseasesmuscle
HM00797FSTL3placentaMESH:D008107Liver Diseaseslung
HM00797FSTL3placentaMESH:D008107Liver Diseasesliver
HM00797FSTL3placentaMESH:D006869Hydronephrosiskidney
HM00797FSTL3placentaMESH:D017093Liver Failure
HM00797FSTL3placentaMESH:D006457Hemoglobinuria, Paroxysmal
HM00797FSTL3placentaMESH:D006505Hepatitis
HM00797FSTL3placentaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM00797FSTL3placentaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM00797FSTL3placentaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM00797FSTL3placentaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM00797FSTL3placentaMESH:D009421Nervous System Malformations
HM00797FSTL3placentaMESH:D007569Jaw Abnormalities
HM00797FSTL3placentaMESH:D004487Edema
HM00797FSTL3placentaMESH:D008103Liver Cirrhosisliver
HM00797FSTL3placentaMESH:D009404Nephrotic Syndromekidney
HM00797FSTL3placentaMESH:D018281Cholangiocarcinomaliver
HM00797FSTL3placentaMESH:D000013Congenital Abnormalities
HM00797FSTL3placentaMESH:D005124Eye Abnormalities
HM00797FSTL3placentaMESH:D018248Adenoma, Liver Cell
HM00797FSTL3placentaMESH:D000740Anemiabone marrow
HM00797FSTL3placentaMESH:D001778Blood Coagulation Disordersbone marrow
HM00797FSTL3placentaMESH:D006470Hemorrhage
HM00797FSTL3placentaMESH:D017114Liver Failure, Acute
HM00797FSTL3placentaMESH:D012878Skin Neoplasms
HM00797FSTL3placentaMESH:D000014Abnormalities, Drug-Induced
HM00797FSTL3placentaMESH:D056486Drug-Induced Liver Injury
HM00797FSTL3placentaMESH:D054079Vascular Malformations
HM00797FSTL3placentaMESH:D007249Inflammation
HM00797FSTL3placentaMESH:D008654Mesotheliomabone
HM00797FSTL3placentaMESH:D019282Wasting Syndrome
HM00797FSTL3placentaMESH:D011565Psoriasisskin
HM00797FSTL3placentaMESH:D012852Sinusitis
HM00797FSTL3placentaMESH:D005313Fetal Death
HM00797FSTL3placentaMESH:D005355Fibrosis
HM00797FSTL3placentaMESH:D002972Cleft Palate
HM00797FSTL3placentaMESH:D010300Parkinson Diseasenerve
HM00797FSTL3placentaMESH:D014605Uveitiseye
HM00797FSTL3placentaMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00797FSTL3placentaMESH:D006330Heart Defects, Congenital
HM00797FSTL3placentaMESH:D008106Liver Cirrhosis, Experimental
HM00797FSTL3placentaMESH:D009402Nephrosis, Lipoidkidney
HM00797FSTL3placentaMESH:D001836Body Weight Changes
HM00797FSTL3placentaMESH:D017119Porphyria Cutanea Tardaskin