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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05009GNAI3esophagusMESH:D008106Liver Cirrhosis, Experimental
HM05009GNAI3esophagusMESH:D010146Pain
HM05009GNAI3esophagusMESH:D015431Weight Loss
HM05009GNAI3esophagusMESH:D014985Xerophthalmiaeye
HM05009GNAI3esophagusMESH:D007248Infertility, Male
HM05009GNAI3esophagusMESH:D008114Liver Neoplasms, Experimental
HM05009GNAI3esophagusMESH:D011014Pneumonialung
HM05009GNAI3esophagusMESH:D000740Anemiabone marrow
HM05009GNAI3esophagusMESH:D002386Cataractpancreas
HM05009GNAI3esophagusMESH:D002386Cataracteye
HM05009GNAI3esophagusMESH:D008175Lung Neoplasmslung
HM05009GNAI3esophagusMESH:D012729Sex Chromosome Aberrations
HM05009GNAI3esophagusMESH:D001321Autistic Disorder
HM05009GNAI3esophagusMESH:D005313Fetal Death
HM05009GNAI3esophagusMESH:D001778Blood Coagulation Disordersbone marrow
HM05009GNAI3esophagusMESH:D007638Keratoconjunctivitis Siccaeye
HM05009GNAI3esophagusMESH:D006869Hydronephrosiskidney
HM05009GNAI3esophagusMESH:D020258Neurotoxicity Syndromes
HM05009GNAI3esophagusMESH:D005885Gingival Hyperplasia
HM05009GNAI3esophagusMESH:D006948Hyperkinesis
HM05009GNAI3esophagusMESH:D006973Hypertensionlung
HM05009GNAI3esophagusMESH:D006973Hypertensionheart
HM05009GNAI3esophagusMESH:D006973Hypertensionblood vessel
HM05009GNAI3esophagusMESH:D012878Skin Neoplasms
HM05009GNAI3esophagusMESH:D003704Dementianerve
HM05009GNAI3esophagusMESH:D003704Dementiablood vessel
HM05009GNAI3esophagusMESH:D011565Psoriasisskin
HM05009GNAI3esophagusMESH:D000014Abnormalities, Drug-Induced
HM05009GNAI3esophagusMESH:D002277Carcinoma
HM05009GNAI3esophagusMESH:D011471Prostatic Neoplasmsprostate
HM05009GNAI3esophagusMESH:D006330Heart Defects, Congenital
HM05009GNAI3esophagusMESH:D006470Hemorrhage
HM05009GNAI3esophagusMESH:D008113Liver Neoplasms
HM05009GNAI3esophagusMESH:D008113Liver Neoplasms
HM05009GNAI3esophagusMESH:D009765Obesity
HM05009GNAI3esophagusMESH:D009421Nervous System Malformations
HM05009GNAI3esophagusMESH:D017119Porphyria Cutanea Tardaskin
HM05009GNAI3esophagusMESH:D012135Respiratory Sounds
HM05009GNAI3esophagusMESH:D012559Schizophrenia
HM05009GNAI3esophagusMESH:D001836Body Weight Changes
HM05009GNAI3esophagusMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05009GNAI3esophagusMESH:D008064Lipidoses
HM05009GNAI3esophagusMESH:D013959Thyroid Diseasesthyroid
HM05009GNAI3esophagusMESH:D009410Nerve Degeneration
HM05009GNAI3esophagusMESH:D004487Edema
HM05009GNAI3esophagusMESH:D011041Poisoning
HM05009GNAI3esophagusMESH:D001327Autoimmune Diseasesskin
HM05009GNAI3esophagusMESH:D001327Autoimmune Diseasesparathyroid gland
HM05009GNAI3esophagusMESH:D001327Autoimmune Diseaseslung
HM05009GNAI3esophagusMESH:D001327Autoimmune Diseaseseye
HM05009GNAI3esophagusMESH:D001327Autoimmune Diseasesbone marrow
HM05009GNAI3esophagusMESH:D050171Dyslipidemias
HM05009GNAI3esophagusMESH:D056486Drug-Induced Liver Injury
HM05009GNAI3esophagusMESH:D001848Bone Diseases, Developmental
HM05009GNAI3esophagusMESH:D008107Liver Diseasesskin
HM05009GNAI3esophagusMESH:D008107Liver Diseasesmuscle
HM05009GNAI3esophagusMESH:D008107Liver Diseaseslung
HM05009GNAI3esophagusMESH:D008107Liver Diseasesliver
HM05009GNAI3esophagusMESH:D000799Angioedemaskin
HM05009GNAI3esophagusMESH:D001523Mental Disorders
HM05009GNAI3esophagusMESH:D014581Urticariaskin
HM05009GNAI3esophagusMESH:D004417Dyspnea
HM05009GNAI3esophagusMESH:D019636Neurodegenerative Diseasesnerve
HM05009GNAI3esophagusMESH:D018281Cholangiocarcinomaliver
HM05009GNAI3esophagusMESH:D008546Melanoma, Experimental
HM05009GNAI3esophagusMESH:D010300Parkinson Diseasenerve
HM05009GNAI3esophagusMESH:D004362Drug Toxicity
HM05009GNAI3esophagusMESH:D010382Peliosis Hepatisliver
HM05009GNAI3esophagusMESH:D000013Congenital Abnormalities
HM05009GNAI3esophagusMESH:D000382Agricultural Workers' Diseases
HM05009GNAI3esophagusMESH:D006332Cardiomegaly
HM05009GNAI3esophagusMESH:D009402Nephrosis, Lipoidkidney
HM05009GNAI3esophagusMESH:D009404Nephrotic Syndromekidney
HM05009GNAI3esophagusMESH:D015619Respiratory System Abnormalities
HM05009GNAI3esophagusMESH:D014605Uveitiseye
HM05009GNAI3esophagusMESH:D005909Glioblastomabone
HM05009GNAI3esophagusMESH:D005909Glioblastomabrain
HM05009GNAI3esophagusMESH:D005909Glioblastomabone
HM05009GNAI3esophagusMESH:D019282Wasting Syndrome
HM05009GNAI3esophagusMESH:D002972Cleft Palate
HM05009GNAI3esophagusMESH:D017180Tachycardia, Ventricular
HM05009GNAI3esophagusMESH:D014570Urologic Diseases
HM05009GNAI3esophagusMESH:D006457Hemoglobinuria, Paroxysmal
HM05009GNAI3esophagusMESH:D006505Hepatitis
HM05009GNAI3esophagusMESH:D006529Hepatomegaly
HM05009GNAI3esophagusMESH:D011658Pulmonary Fibrosislung
HM05009GNAI3esophagusMESH:D054079Vascular Malformations
HM05009GNAI3esophagusMESH:D012162Retinal Degenerationeye
HM05009GNAI3esophagusMESH:D003072Cognition Disorders
HM05009GNAI3esophagusMESH:D005355Fibrosis
HM05009GNAI3esophagusMESH:D007674Kidney Diseasesureter
HM05009GNAI3esophagusMESH:D007674Kidney Diseasespituitary
HM05009GNAI3esophagusMESH:D007674Kidney Diseaseskidney
HM05009GNAI3esophagusMESH:D018248Adenoma, Liver Cell
HM05009GNAI3esophagusMESH:D017202Myocardial Ischemiaheart
HM05009GNAI3esophagusMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM05009GNAI3esophagusMESH:D011595Psychomotor Agitation
HM05009GNAI3esophagusMESH:D012128Respiratory Distress Syndrome, Adultlung
HM05009GNAI3esophagusMESH:D019465Craniofacial Abnormalities
HM05009GNAI3esophagusMESH:D011618Psychotic Disorders
HM05009GNAI3esophagusMESH:D006970Disorders of Excessive Somnolence
HM05009GNAI3esophagusMESH:D017114Liver Failure, Acute
HM05009GNAI3esophagusMESH:D005911Gliosis
HM05009GNAI3esophagusMESH:D012140Respiratory Tract Diseases
HM05009GNAI3esophagusMESH:D006930Hyperalgesia
HM05009GNAI3esophagusMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05009GNAI3esophagusMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05009GNAI3esophagusMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05009GNAI3esophagusMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05009GNAI3esophagusMESH:D015430Weight Gain
HM05009GNAI3esophagusMESH:D002375Catalepsy
HM05009GNAI3esophagusMESH:D005124Eye Abnormalities
HM05009GNAI3esophagusMESH:D000380Agranulocytosisbone marrow
HM05009GNAI3esophagusMESH:D007569Jaw Abnormalities
HM05009GNAI3esophagusMESH:D024821Metabolic Syndrome X
HM05009GNAI3esophagusMESH:D016757Death, Sudden, Cardiac
HM05009GNAI3esophagusMESH:D011297Prenatal Exposure Delayed Effects
HM05009GNAI3esophagusMESH:D004489Edema, Cardiac
HM05009GNAI3esophagusMESH:D007249Inflammation
HM05009GNAI3esophagusMESH:D001943Breast Neoplasmsbreast