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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05057CEP152liverMESH:D015428Myocardial Reperfusion Injury
HM05057CEP152liverMESH:D009410Nerve Degeneration
HM05057CEP152liverMESH:D008113Liver Neoplasms
HM05057CEP152liverMESH:D008113Liver Neoplasms
HM05057CEP152liverMESH:D008106Liver Cirrhosis, Experimental
HM05057CEP152liverMESH:D006529Hepatomegaly
HM05057CEP152liverMESH:D055371Acute Lung Injury
HM05057CEP152liverMESH:D009765Obesity
HM05057CEP152liverMESH:D005234Fatty Liver
HM05057CEP152liverMESH:D007333Insulin Resistance
HM05057CEP152liverMESH:D015427Reperfusion Injury
HM05057CEP152liverMESH:D018248Adenoma, Liver Cell
HM05057CEP152liverOMIM:604321MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 4
HM05057CEP152liverMESH:D003876Dermatitis, Atopicskin
HM05057CEP152liverMESH:D001778Blood Coagulation Disordersbone marrow
HM05057CEP152liverMESH:D010300Parkinson Diseasenerve
HM05057CEP152liverMESH:D004487Edema
HM05057CEP152liverMESH:D006333Heart Failureheart
HM05057CEP152liverMESH:D006943Hyperglycemia
HM05057CEP152liverMESH:D009203Myocardial Infarctionheart
HM05057CEP152liverMESH:D020734Parkinsonian Disorders
HM05057CEP152liverMESH:D002779Cholestasisliver
HM05057CEP152liverMESH:D009135Muscular Diseasesmuscle
HM05057CEP152liverMESH:D009369Neoplasmsspleen
HM05057CEP152liverMESH:D009369Neoplasmsbone marrow
HM05057CEP152liverMESH:C537533Seckel syndrome 1