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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05358KELspleenMESH:D006332Cardiomegaly
HM05358KELspleenMESH:D012878Skin Neoplasms
HM05358KELspleenMESH:D001836Body Weight Changes
HM05358KELspleenMESH:D010146Pain
HM05358KELspleenMESH:D018281Cholangiocarcinomaliver
HM05358KELspleenMESH:D000013Congenital Abnormalities
HM05358KELspleenMESH:D007674Kidney Diseasesureter
HM05358KELspleenMESH:D007674Kidney Diseasespituitary
HM05358KELspleenMESH:D007674Kidney Diseaseskidney
HM05358KELspleenMESH:D001321Autistic Disorder
HM05358KELspleenMESH:D001848Bone Diseases, Developmental
HM05358KELspleenMESH:D008106Liver Cirrhosis, Experimental
HM05358KELspleenMESH:D018248Adenoma, Liver Cell
HM05358KELspleenMESH:D000799Angioedemaskin
HM05358KELspleenMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05358KELspleenMESH:D009421Nervous System Malformations
HM05358KELspleenMESH:D017202Myocardial Ischemiaheart
HM05358KELspleenMESH:D011297Prenatal Exposure Delayed Effects
HM05358KELspleenMESH:D001778Blood Coagulation Disordersbone marrow
HM05358KELspleenMESH:D056486Drug-Induced Liver Injury
HM05358KELspleenMESH:D014581Urticariaskin
HM05358KELspleenMESH:D000740Anemiabone marrow
HM05358KELspleenMESH:D005355Fibrosis
HM05358KELspleenMESH:D012162Retinal Degenerationeye
HM05358KELspleenMESH:D007569Jaw Abnormalities
HM05358KELspleenMESH:D012128Respiratory Distress Syndrome, Adultlung
HM05358KELspleenMESH:D012135Respiratory Sounds
HM05358KELspleenMESH:D004489Edema, Cardiac
HM05358KELspleenMESH:D010382Peliosis Hepatisliver
HM05358KELspleenMESH:D017114Liver Failure, Acute
HM05358KELspleenMESH:D002386Cataractpancreas
HM05358KELspleenMESH:D002386Cataracteye
HM05358KELspleenMESH:D008107Liver Diseasesskin
HM05358KELspleenMESH:D008107Liver Diseasesmuscle
HM05358KELspleenMESH:D008107Liver Diseaseslung
HM05358KELspleenMESH:D008107Liver Diseasesliver
HM05358KELspleenMESH:D019465Craniofacial Abnormalities
HM05358KELspleenMESH:D008175Lung Neoplasmslung
HM05358KELspleenMESH:D000014Abnormalities, Drug-Induced
HM05358KELspleenMESH:D017119Porphyria Cutanea Tardaskin
HM05358KELspleenMESH:D015619Respiratory System Abnormalities
HM05358KELspleenMESH:D005313Fetal Death
HM05358KELspleenMESH:D054079Vascular Malformations
HM05358KELspleenMESH:D002277Carcinoma
HM05358KELspleenMESH:D006930Hyperalgesia
HM05358KELspleenMESH:D005911Gliosis
HM05358KELspleenMESH:D007248Infertility, Male
HM05358KELspleenMESH:D008546Melanoma, Experimental
HM05358KELspleenMESH:D001943Breast Neoplasmsbreast
HM05358KELspleenMESH:D019636Neurodegenerative Diseasesnerve
HM05358KELspleenMESH:D010300Parkinson Diseasenerve
HM05358KELspleenMESH:D013272Stomach Diseasesblood vessel
HM05358KELspleenMESH:D000382Agricultural Workers' Diseases
HM05358KELspleenMESH:D006973Hypertensionlung
HM05358KELspleenMESH:D006973Hypertensionheart
HM05358KELspleenMESH:D006973Hypertensionblood vessel
HM05358KELspleenMESH:D013959Thyroid Diseasesthyroid
HM05358KELspleenMESH:D006330Heart Defects, Congenital
HM05358KELspleenMESH:D019282Wasting Syndrome
HM05358KELspleenMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM05358KELspleenMESH:D011658Pulmonary Fibrosislung
HM05358KELspleenMESH:D013276Stomach Ulcer
HM05358KELspleenMESH:D004362Drug Toxicity
HM05358KELspleenMESH:D002972Cleft Palate
HM05358KELspleenMESH:D006869Hydronephrosiskidney
HM05358KELspleenMESH:D009410Nerve Degeneration
HM05358KELspleenMESH:D008113Liver Neoplasms
HM05358KELspleenMESH:D008113Liver Neoplasms
HM05358KELspleenMESH:D005124Eye Abnormalities
HM05358KELspleenMESH:D006529Hepatomegaly
HM05358KELspleenMESH:D008114Liver Neoplasms, Experimental
HM05358KELspleenMESH:D004487Edema
HM05358KELspleenMESH:D007249Inflammation
HM05358KELspleenMESH:D011014Pneumonialung
HM05358KELspleenMESH:D006470Hemorrhage