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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01634CFC1pancreasOMIM:217095CONOTRUNCAL HEART MALFORMATIONS
HM01634CFC1pancreasMESH:D017114Liver Failure, Acute
HM01634CFC1pancreasMESH:D008546Melanoma, Experimental
HM01634CFC1pancreasOMIM:605376HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HM01634CFC1pancreasMESH:D007674Kidney Diseasesureter
HM01634CFC1pancreasMESH:D007674Kidney Diseasespituitary
HM01634CFC1pancreasMESH:D007674Kidney Diseaseskidney
HM01634CFC1pancreasMESH:D002386Cataractpancreas
HM01634CFC1pancreasMESH:D002386Cataracteye
HM01634CFC1pancreasMESH:D014188Transposition of Great Vessels
HM01634CFC1pancreasMESH:D056486Drug-Induced Liver Injury
HM01634CFC1pancreasMESH:D014581Urticariaskin
HM01634CFC1pancreasMESH:D019636Neurodegenerative Diseasesnerve
HM01634CFC1pancreasMESH:D010146Pain
HM01634CFC1pancreasMESH:D008107Liver Diseasesskin
HM01634CFC1pancreasMESH:D008107Liver Diseasesmuscle
HM01634CFC1pancreasMESH:D008107Liver Diseaseslung
HM01634CFC1pancreasMESH:D008107Liver Diseasesliver
HM01634CFC1pancreasMESH:D000799Angioedemaskin
HM01634CFC1pancreasMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01634CFC1pancreasMESH:D001321Autistic Disorder
HM01634CFC1pancreasMESH:D006930Hyperalgesia