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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05035TNXBthyroidMESH:D005355Fibrosis
HM05035TNXBthyroidMESH:C536193Ehlers-Danlos syndrome caused by tenascin-X deficiency
HM05035TNXBthyroidMESH:D006932Hyperbilirubinemia
HM05035TNXBthyroidMESH:D020734Parkinsonian Disorders
HM05035TNXBthyroidMESH:D056486Drug-Induced Liver Injury
HM05035TNXBthyroidMESH:D008107Liver Diseasesskin
HM05035TNXBthyroidMESH:D008107Liver Diseasesmuscle
HM05035TNXBthyroidMESH:D008107Liver Diseaseslung
HM05035TNXBthyroidMESH:D008107Liver Diseasesliver
HM05035TNXBthyroidMESH:C536196Ehlers-Danlos syndrome type 3
HM05035TNXBthyroidMESH:D011658Pulmonary Fibrosislung
HM05035TNXBthyroidMESH:D004890Erythema
HM05035TNXBthyroidMESH:D004487Edema
HM05035TNXBthyroidMESH:D017093Liver Failure
HM05035TNXBthyroidMESH:D006505Hepatitis
HM05035TNXBthyroidMESH:D005234Fatty Liver
HM05035TNXBthyroidMESH:D001989Bronchiolitis Obliteranslung
HM05035TNXBthyroidMESH:D008114Liver Neoplasms, Experimental
HM05035TNXBthyroidMESH:D008106Liver Cirrhosis, Experimental
HM05035TNXBthyroidMESH:D017114Liver Failure, Acute
HM05035TNXBthyroidMESH:D011041Poisoning
HM05035TNXBthyroidMESH:D007249Inflammation
HM05035TNXBthyroidMESH:D008171Lung Diseases
HM05035TNXBthyroidMESH:D010300Parkinson Diseasenerve
HM05035TNXBthyroidMESH:D012871Skin Diseasesskin
HM05035TNXBthyroidMESH:D008103Liver Cirrhosisliver
HM05035TNXBthyroidMESH:D011537Pruritus
HM05035TNXBthyroidMESH:D029481Bronchitis, Chroniclung
HM05035TNXBthyroidMESH:D001249Asthmalung
HM05035TNXBthyroidMESH:D002252Carbon Tetrachloride Poisoning
HM05035TNXBthyroidMESH:D008175Lung Neoplasmslung
HM05035TNXBthyroidMESH:D009503Neutropeniabone marrow
HM05035TNXBthyroidMESH:D001768Blister
HM05035TNXBthyroidMESH:D009410Nerve Degeneration