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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01788PTPRCAPtonsilMESH:D002386Cataractpancreas
HM01788PTPRCAPtonsilMESH:D002386Cataracteye
HM01788PTPRCAPtonsilMESH:D002100Cachexia
HM01788PTPRCAPtonsilMESH:D019636Neurodegenerative Diseasesnerve
HM01788PTPRCAPtonsilMESH:D008546Melanoma, Experimental
HM01788PTPRCAPtonsilMESH:D010146Pain
HM01788PTPRCAPtonsilMESH:D011014Pneumonialung
HM01788PTPRCAPtonsilMESH:D000544Alzheimer Diseasenerve
HM01788PTPRCAPtonsilMESH:D001321Autistic Disorder
HM01788PTPRCAPtonsilMESH:D001249Asthmalung
HM01788PTPRCAPtonsilMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01788PTPRCAPtonsilMESH:D001172Arthritis, Rheumatoidbone
HM01788PTPRCAPtonsilMESH:D007674Kidney Diseasesureter
HM01788PTPRCAPtonsilMESH:D007674Kidney Diseasespituitary
HM01788PTPRCAPtonsilMESH:D007674Kidney Diseaseskidney
HM01788PTPRCAPtonsilMESH:D000799Angioedemaskin
HM01788PTPRCAPtonsilMESH:D002658Developmental Disabilities
HM01788PTPRCAPtonsilMESH:D008171Lung Diseases
HM01788PTPRCAPtonsilMESH:D014581Urticariaskin
HM01788PTPRCAPtonsilMESH:D056486Drug-Induced Liver Injury
HM01788PTPRCAPtonsilMESH:D008679Metaplasia
HM01788PTPRCAPtonsilMESH:D017114Liver Failure, Acute
HM01788PTPRCAPtonsilMESH:D006930Hyperalgesia
HM01788PTPRCAPtonsilMESH:D010538Peritonitis
HM01788PTPRCAPtonsilMESH:D016535Bronchial Hyperreactivity
HM01788PTPRCAPtonsilMESH:D008175Lung Neoplasmslung
HM01788PTPRCAPtonsilMESH:D008107Liver Diseasesskin
HM01788PTPRCAPtonsilMESH:D008107Liver Diseasesmuscle
HM01788PTPRCAPtonsilMESH:D008107Liver Diseaseslung
HM01788PTPRCAPtonsilMESH:D008107Liver Diseasesliver