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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02700C10orf2lymphMESH:D000013Congenital Abnormalities
HM02700C10orf2lymphMESH:D007569Jaw Abnormalities
HM02700C10orf2lymphOMIM:609286PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 3
HM02700C10orf2lymphMESH:C537583Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
HM02700C10orf2lymphMESH:D018281Cholangiocarcinomaliver
HM02700C10orf2lymphMESH:D006330Heart Defects, Congenital
HM02700C10orf2lymphMESH:D008175Lung Neoplasmslung
HM02700C10orf2lymphMESH:D001778Blood Coagulation Disordersbone marrow
HM02700C10orf2lymphMESH:D019282Wasting Syndrome
HM02700C10orf2lymphMESH:D002972Cleft Palate
HM02700C10orf2lymphMESH:D006332Cardiomegaly
HM02700C10orf2lymphMESH:D018248Adenoma, Liver Cell
HM02700C10orf2lymphMESH:D000740Anemiabone marrow
HM02700C10orf2lymphMESH:D001836Body Weight Changes
HM02700C10orf2lymphMESH:D005124Eye Abnormalities
HM02700C10orf2lymphMESH:D017119Porphyria Cutanea Tardaskin
HM02700C10orf2lymphMESH:D015619Respiratory System Abnormalities
HM02700C10orf2lymphMESH:D005355Fibrosis
HM02700C10orf2lymphMESH:D009421Nervous System Malformations
HM02700C10orf2lymphMESH:D008113Liver Neoplasms
HM02700C10orf2lymphMESH:D008113Liver Neoplasms
HM02700C10orf2lymphMESH:D001943Breast Neoplasmsbreast
HM02700C10orf2lymphMESH:D008114Liver Neoplasms, Experimental
HM02700C10orf2lymphMESH:D002277Carcinoma
HM02700C10orf2lymphMESH:D019465Craniofacial Abnormalities
HM02700C10orf2lymphMESH:D004489Edema, Cardiac
HM02700C10orf2lymphMESH:D008106Liver Cirrhosis, Experimental
HM02700C10orf2lymphOMIM:251880MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
HM02700C10orf2lymphOMIM:271245MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)
HM02700C10orf2lymphMESH:D011297Prenatal Exposure Delayed Effects
HM02700C10orf2lymphMESH:D004487Edema
HM02700C10orf2lymphMESH:D017202Myocardial Ischemiaheart
HM02700C10orf2lymphMESH:D056486Drug-Induced Liver Injury
HM02700C10orf2lymphMESH:D006529Hepatomegaly
HM02700C10orf2lymphMESH:D054079Vascular Malformations
HM02700C10orf2lymphMESH:D004362Drug Toxicity
HM02700C10orf2lymphMESH:D007249Inflammation
HM02700C10orf2lymphMESH:D006973Hypertensionlung
HM02700C10orf2lymphMESH:D006973Hypertensionheart
HM02700C10orf2lymphMESH:D006973Hypertensionblood vessel
HM02700C10orf2lymphMESH:D000014Abnormalities, Drug-Induced
HM02700C10orf2lymphMESH:D010382Peliosis Hepatisliver
HM02700C10orf2lymphMESH:D003924Diabetes Mellitus, Type 2pancreas
HM02700C10orf2lymphMESH:D013959Thyroid Diseasesthyroid
HM02700C10orf2lymphMESH:D005313Fetal Death
HM02700C10orf2lymphMESH:D012878Skin Neoplasms
HM02700C10orf2lymphMESH:D006869Hydronephrosiskidney
HM02700C10orf2lymphMESH:D006470Hemorrhage
HM02700C10orf2lymphMESH:D001848Bone Diseases, Developmental