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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00536NDUFAF2blood vesselMESH:D008175Lung Neoplasmslung
HM00536NDUFAF2blood vesselMESH:D015619Respiratory System Abnormalities
HM00536NDUFAF2blood vesselMESH:D011297Prenatal Exposure Delayed Effects
HM00536NDUFAF2blood vesselMESH:D004489Edema, Cardiac
HM00536NDUFAF2blood vesselMESH:D006973Hypertensionlung
HM00536NDUFAF2blood vesselMESH:D006973Hypertensionheart
HM00536NDUFAF2blood vesselMESH:D006973Hypertensionblood vessel
HM00536NDUFAF2blood vesselMESH:D017119Porphyria Cutanea Tardaskin
HM00536NDUFAF2blood vesselMESH:D006470Hemorrhage
HM00536NDUFAF2blood vesselMESH:D012878Skin Neoplasms
HM00536NDUFAF2blood vesselMESH:D005355Fibrosis
HM00536NDUFAF2blood vesselMESH:D001848Bone Diseases, Developmental
HM00536NDUFAF2blood vesselMESH:D006330Heart Defects, Congenital
HM00536NDUFAF2blood vesselMESH:D001943Breast Neoplasmsbreast
HM00536NDUFAF2blood vesselMESH:D019282Wasting Syndrome
HM00536NDUFAF2blood vesselMESH:D000014Abnormalities, Drug-Induced
HM00536NDUFAF2blood vesselMESH:D004362Drug Toxicity
HM00536NDUFAF2blood vesselMESH:D008106Liver Cirrhosis, Experimental
HM00536NDUFAF2blood vesselMESH:D008113Liver Neoplasms
HM00536NDUFAF2blood vesselMESH:D008113Liver Neoplasms
HM00536NDUFAF2blood vesselMESH:D018248Adenoma, Liver Cell
HM00536NDUFAF2blood vesselMESH:D054079Vascular Malformations
HM00536NDUFAF2blood vesselMESH:D018281Cholangiocarcinomaliver
HM00536NDUFAF2blood vesselMESH:D000740Anemiabone marrow
HM00536NDUFAF2blood vesselMESH:D006869Hydronephrosiskidney
HM00536NDUFAF2blood vesselMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00536NDUFAF2blood vesselMESH:D007249Inflammation
HM00536NDUFAF2blood vesselMESH:D001778Blood Coagulation Disordersbone marrow
HM00536NDUFAF2blood vesselMESH:D013959Thyroid Diseasesthyroid
HM00536NDUFAF2blood vesselMESH:D007569Jaw Abnormalities
HM00536NDUFAF2blood vesselMESH:D004487Edema
HM00536NDUFAF2blood vesselMESH:D002972Cleft Palate
HM00536NDUFAF2blood vesselMESH:D017202Myocardial Ischemiaheart
HM00536NDUFAF2blood vesselMESH:D005313Fetal Death
HM00536NDUFAF2blood vesselMESH:D010382Peliosis Hepatisliver
HM00536NDUFAF2blood vesselMESH:D008114Liver Neoplasms, Experimental
HM00536NDUFAF2blood vesselMESH:D006332Cardiomegaly
HM00536NDUFAF2blood vesselOMIM:252010MITOCHONDRIAL COMPLEX I DEFICIENCY
HM00536NDUFAF2blood vesselMESH:D009421Nervous System Malformations
HM00536NDUFAF2blood vesselMESH:D002277Carcinoma
HM00536NDUFAF2blood vesselMESH:D000013Congenital Abnormalities
HM00536NDUFAF2blood vesselMESH:D001836Body Weight Changes
HM00536NDUFAF2blood vesselMESH:D019465Craniofacial Abnormalities
HM00536NDUFAF2blood vesselMESH:D007888Leigh Disease
HM00536NDUFAF2blood vesselMESH:D005124Eye Abnormalities
HM00536NDUFAF2blood vesselMESH:D056486Drug-Induced Liver Injury
HM00536NDUFAF2blood vesselMESH:D006529Hepatomegaly