Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01639NOTUMplacentaMESH:D004487Edema
HM01639NOTUMplacentaMESH:D017114Liver Failure, Acute
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseasesspinal cord
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseasesskin
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseasesnerve
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseasesmuscle
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseaseseye
HM01639NOTUMplacentaMESH:D002493Central Nervous System Diseasesbrain
HM01639NOTUMplacentaMESH:D004831Epilepsies, Myoclonicmuscle
HM01639NOTUMplacentaMESH:D018248Adenoma, Liver Cell
HM01639NOTUMplacentaMESH:D008107Liver Diseasesskin
HM01639NOTUMplacentaMESH:D008107Liver Diseasesmuscle
HM01639NOTUMplacentaMESH:D008107Liver Diseaseslung
HM01639NOTUMplacentaMESH:D008107Liver Diseasesliver
HM01639NOTUMplacentaMESH:D006332Cardiomegaly
HM01639NOTUMplacentaMESH:D005885Gingival Hyperplasia
HM01639NOTUMplacentaMESH:D000013Congenital Abnormalities
HM01639NOTUMplacentaMESH:D017119Porphyria Cutanea Tardaskin
HM01639NOTUMplacentaMESH:D012640Seizuresmuscle
HM01639NOTUMplacentaMESH:D008546Melanoma, Experimental
HM01639NOTUMplacentaMESH:D010382Peliosis Hepatisliver
HM01639NOTUMplacentaMESH:D004421Dystonia
HM01639NOTUMplacentaMESH:D006930Hyperalgesia
HM01639NOTUMplacentaMESH:D000799Angioedemaskin
HM01639NOTUMplacentaMESH:D007674Kidney Diseasesureter
HM01639NOTUMplacentaMESH:D007674Kidney Diseasespituitary
HM01639NOTUMplacentaMESH:D007674Kidney Diseaseskidney
HM01639NOTUMplacentaMESH:D009402Nephrosis, Lipoidkidney
HM01639NOTUMplacentaMESH:D007569Jaw Abnormalities
HM01639NOTUMplacentaMESH:D006973Hypertensionlung
HM01639NOTUMplacentaMESH:D006973Hypertensionheart
HM01639NOTUMplacentaMESH:D006973Hypertensionblood vessel
HM01639NOTUMplacentaMESH:D008114Liver Neoplasms, Experimental
HM01639NOTUMplacentaMESH:D014985Xerophthalmiaeye
HM01639NOTUMplacentaMESH:D002386Cataractpancreas
HM01639NOTUMplacentaMESH:D002386Cataracteye
HM01639NOTUMplacentaMESH:D010190Pancreatic Neoplasmspancreas
HM01639NOTUMplacentaMESH:D006528Carcinoma, Hepatocellularliver
HM01639NOTUMplacentaMESH:D000740Anemiabone marrow
HM01639NOTUMplacentaMESH:D006457Hemoglobinuria, Paroxysmal
HM01639NOTUMplacentaMESH:D019636Neurodegenerative Diseasesnerve
HM01639NOTUMplacentaMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01639NOTUMplacentaMESH:D019465Craniofacial Abnormalities
HM01639NOTUMplacentaMESH:D010146Pain
HM01639NOTUMplacentaMESH:D006470Hemorrhage
HM01639NOTUMplacentaMESH:D020191Myoclonic Epilepsies, Progressivenerve
HM01639NOTUMplacentaMESH:D020191Myoclonic Epilepsies, Progressivemuscle
HM01639NOTUMplacentaMESH:D009421Nervous System Malformations
HM01639NOTUMplacentaMESH:D006869Hydronephrosiskidney
HM01639NOTUMplacentaMESH:D007638Keratoconjunctivitis Siccaeye
HM01639NOTUMplacentaMESH:D004362Drug Toxicity
HM01639NOTUMplacentaMESH:D018281Cholangiocarcinomaliver
HM01639NOTUMplacentaMESH:D056486Drug-Induced Liver Injury
HM01639NOTUMplacentaMESH:D011565Psoriasisskin
HM01639NOTUMplacentaMESH:D004832Epilepsy, Absencemuscle
HM01639NOTUMplacentaMESH:D015619Respiratory System Abnormalities
HM01639NOTUMplacentaMESH:D013959Thyroid Diseasesthyroid
HM01639NOTUMplacentaMESH:D000014Abnormalities, Drug-Induced
HM01639NOTUMplacentaMESH:D001778Blood Coagulation Disordersbone marrow
HM01639NOTUMplacentaMESH:D001848Bone Diseases, Developmental
HM01639NOTUMplacentaMESH:D004828Epilepsies, Partialmuscle
HM01639NOTUMplacentaMESH:D005355Fibrosis
HM01639NOTUMplacentaMESH:D007249Inflammation
HM01639NOTUMplacentaMESH:D002972Cleft Palate
HM01639NOTUMplacentaMESH:D008113Liver Neoplasms
HM01639NOTUMplacentaMESH:D008113Liver Neoplasms
HM01639NOTUMplacentaMESH:D008106Liver Cirrhosis, Experimental
HM01639NOTUMplacentaMESH:D017202Myocardial Ischemiaheart
HM01639NOTUMplacentaMESH:D004489Edema, Cardiac
HM01639NOTUMplacentaMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01639NOTUMplacentaMESH:D009404Nephrotic Syndromekidney
HM01639NOTUMplacentaMESH:D014605Uveitiseye
HM01639NOTUMplacentaMESH:D005124Eye Abnormalities
HM01639NOTUMplacentaMESH:D006529Hepatomegaly
HM01639NOTUMplacentaMESH:D019310Pseudolymphoma
HM01639NOTUMplacentaMESH:D054079Vascular Malformations
HM01639NOTUMplacentaMESH:D019282Wasting Syndrome
HM01639NOTUMplacentaMESH:D017029Epilepsy, Complex Partialmuscle
HM01639NOTUMplacentaMESH:D012878Skin Neoplasms
HM01639NOTUMplacentaMESH:D004827Epilepsymuscle
HM01639NOTUMplacentaMESH:D010018Osteomalaciabone
HM01639NOTUMplacentaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01639NOTUMplacentaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01639NOTUMplacentaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01639NOTUMplacentaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01639NOTUMplacentaMESH:D011297Prenatal Exposure Delayed Effects
HM01639NOTUMplacentaMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01639NOTUMplacentaMESH:D003294Seizures, Febrile
HM01639NOTUMplacentaMESH:D014581Urticariaskin
HM01639NOTUMplacentaMESH:D001836Body Weight Changes
HM01639NOTUMplacentaMESH:D005313Fetal Death
HM01639NOTUMplacentaMESH:D006330Heart Defects, Congenital
HM01639NOTUMplacentaMESH:D008175Lung Neoplasmslung
HM01639NOTUMplacentaMESH:D001943Breast Neoplasmsbreast
HM01639NOTUMplacentaMESH:D011230Precancerous Conditions
HM01639NOTUMplacentaMESH:D001321Autistic Disorder
HM01639NOTUMplacentaMESH:D002277Carcinoma