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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05991VPS13DlarynxMESH:D001778Blood Coagulation Disordersbone marrow
HM05991VPS13DlarynxMESH:D011297Prenatal Exposure Delayed Effects
HM05991VPS13DlarynxMESH:D001836Body Weight Changes
HM05991VPS13DlarynxMESH:D005234Fatty Liver
HM05991VPS13DlarynxMESH:D007249Inflammation
HM05991VPS13DlarynxMESH:D006869Hydronephrosiskidney
HM05991VPS13DlarynxMESH:D018248Adenoma, Liver Cell
HM05991VPS13DlarynxMESH:D009203Myocardial Infarctionheart
HM05991VPS13DlarynxMESH:D017119Porphyria Cutanea Tardaskin
HM05991VPS13DlarynxMESH:D055371Acute Lung Injury
HM05991VPS13DlarynxMESH:D019584Hot Flashes
HM05991VPS13DlarynxMESH:D006943Hyperglycemia
HM05991VPS13DlarynxMESH:D001848Bone Diseases, Developmental
HM05991VPS13DlarynxMESH:D056486Drug-Induced Liver Injury
HM05991VPS13DlarynxMESH:D000014Abnormalities, Drug-Induced
HM05991VPS13DlarynxMESH:D007251Influenza, Human
HM05991VPS13DlarynxMESH:D010382Peliosis Hepatisliver
HM05991VPS13DlarynxMESH:D013959Thyroid Diseasesthyroid
HM05991VPS13DlarynxMESH:D009421Nervous System Malformations
HM05991VPS13DlarynxMESH:D020521Strokeblood vessel
HM05991VPS13DlarynxMESH:D007674Kidney Diseasesureter
HM05991VPS13DlarynxMESH:D007674Kidney Diseasespituitary
HM05991VPS13DlarynxMESH:D007674Kidney Diseaseskidney
HM05991VPS13DlarynxMESH:D007333Insulin Resistance
HM05991VPS13DlarynxMESH:D008106Liver Cirrhosis, Experimental
HM05991VPS13DlarynxMESH:D004489Edema, Cardiac
HM05991VPS13DlarynxMESH:D002972Cleft Palate
HM05991VPS13DlarynxMESH:D009765Obesity
HM05991VPS13DlarynxMESH:D012878Skin Neoplasms
HM05991VPS13DlarynxMESH:D006973Hypertensionlung
HM05991VPS13DlarynxMESH:D006973Hypertensionheart
HM05991VPS13DlarynxMESH:D006973Hypertensionblood vessel
HM05991VPS13DlarynxMESH:D019465Craniofacial Abnormalities
HM05991VPS13DlarynxMESH:D006529Hepatomegaly
HM05991VPS13DlarynxMESH:D008113Liver Neoplasms
HM05991VPS13DlarynxMESH:D008113Liver Neoplasms
HM05991VPS13DlarynxMESH:D000013Congenital Abnormalities
HM05991VPS13DlarynxMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05991VPS13DlarynxMESH:D006330Heart Defects, Congenital
HM05991VPS13DlarynxMESH:D008171Lung Diseases
HM05991VPS13DlarynxMESH:D008175Lung Neoplasmslung
HM05991VPS13DlarynxMESH:D003876Dermatitis, Atopicskin
HM05991VPS13DlarynxMESH:D011471Prostatic Neoplasmsprostate
HM05991VPS13DlarynxMESH:D017202Myocardial Ischemiaheart
HM05991VPS13DlarynxMESH:D002779Cholestasisliver
HM05991VPS13DlarynxMESH:D001943Breast Neoplasmsbreast
HM05991VPS13DlarynxMESH:D004362Drug Toxicity
HM05991VPS13DlarynxMESH:D009369Neoplasmsspleen
HM05991VPS13DlarynxMESH:D009369Neoplasmsbone marrow
HM05991VPS13DlarynxMESH:D009135Muscular Diseasesmuscle
HM05991VPS13DlarynxMESH:D015428Myocardial Reperfusion Injury
HM05991VPS13DlarynxMESH:D006332Cardiomegaly
HM05991VPS13DlarynxMESH:D000740Anemiabone marrow
HM05991VPS13DlarynxMESH:D005124Eye Abnormalities
HM05991VPS13DlarynxMESH:D006333Heart Failureheart
HM05991VPS13DlarynxMESH:D005355Fibrosis
HM05991VPS13DlarynxMESH:D006470Hemorrhage
HM05991VPS13DlarynxMESH:D002252Carbon Tetrachloride Poisoning
HM05991VPS13DlarynxMESH:D019282Wasting Syndrome
HM05991VPS13DlarynxMESH:D006548Hernia, Diaphragmatic
HM05991VPS13DlarynxMESH:D015619Respiratory System Abnormalities
HM05991VPS13DlarynxMESH:D007569Jaw Abnormalities
HM05991VPS13DlarynxMESH:D015427Reperfusion Injury
HM05991VPS13DlarynxMESH:D018281Cholangiocarcinomaliver
HM05991VPS13DlarynxMESH:D005313Fetal Death
HM05991VPS13DlarynxMESH:D004487Edema
HM05991VPS13DlarynxMESH:D008114Liver Neoplasms, Experimental
HM05991VPS13DlarynxMESH:D002277Carcinoma
HM05991VPS13DlarynxMESH:D054079Vascular Malformations