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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04088EDEM2lymphMESH:D000015Abnormalities, Multiple
HM04088EDEM2lymphMESH:D009404Nephrotic Syndromekidney
HM04088EDEM2lymphMESH:D013226Status Epilepticusmuscle
HM04088EDEM2lymphMESH:D013226Status Epilepticusmuscle
HM04088EDEM2lymphMESH:D013226Status Epilepticusmuscle
HM04088EDEM2lymphMESH:D004831Epilepsies, Myoclonicmuscle
HM04088EDEM2lymphMESH:D004828Epilepsies, Partialmuscle
HM04088EDEM2lymphMESH:D004827Epilepsymuscle
HM04088EDEM2lymphMESH:D005234Fatty Liver
HM04088EDEM2lymphMESH:D005315Fetal Diseases
HM04088EDEM2lymphMESH:D005317Fetal Growth Retardation
HM04088EDEM2lymphMESH:D007638Keratoconjunctivitis Siccaeye
HM04088EDEM2lymphMESH:D007674Kidney Diseasesureter
HM04088EDEM2lymphMESH:D007674Kidney Diseasespituitary
HM04088EDEM2lymphMESH:D007674Kidney Diseaseskidney
HM04088EDEM2lymphMESH:D001848Bone Diseases, Developmental
HM04088EDEM2lymphMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM04088EDEM2lymphMESH:D014564Urogenital Abnormalities
HM04088EDEM2lymphMESH:D009402Nephrosis, Lipoidkidney
HM04088EDEM2lymphMESH:D014605Uveitiseye
HM04088EDEM2lymphMESH:D000550Amblyopiabrain
HM04088EDEM2lymphMESH:D000550Amblyopiabrain
HM04088EDEM2lymphMESH:D012208Rhabdomyosarcomarectum
HM04088EDEM2lymphMESH:D012208Rhabdomyosarcomaprostate
HM04088EDEM2lymphMESH:D012208Rhabdomyosarcomamuscle
HM04088EDEM2lymphMESH:D004832Epilepsy, Absencemuscle
HM04088EDEM2lymphMESH:D017563Lung Diseases, Interstitiallung
HM04088EDEM2lymphMESH:D020194Unverricht-Lundborg Syndromemuscle
HM04088EDEM2lymphMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM04088EDEM2lymphMESH:D009190Myelodysplastic Syndromes
HM04088EDEM2lymphMESH:D004421Dystonia
HM04088EDEM2lymphMESH:D001321Autistic Disorder
HM04088EDEM2lymphMESH:D016135Spinal Dysraphismspinal cord
HM04088EDEM2lymphMESH:D009139Musculoskeletal Abnormalities
HM04088EDEM2lymphMESH:D001008Anxiety Disorders
HM04088EDEM2lymphMESH:D019465Craniofacial Abnormalities
HM04088EDEM2lymphMESH:D000014Abnormalities, Drug-Induced
HM04088EDEM2lymphMESH:D001714Bipolar Disorder
HM04088EDEM2lymphMESH:D014178Translocation, Genetic
HM04088EDEM2lymphMESH:D006457Hemoglobinuria, Paroxysmal
HM04088EDEM2lymphMESH:D017029Epilepsy, Complex Partialmuscle
HM04088EDEM2lymphMESH:D012559Schizophrenia
HM04088EDEM2lymphMESH:D006849Hydrocephalusbrain
HM04088EDEM2lymphMESH:D009436Neural Tube Defects
HM04088EDEM2lymphMESH:D006973Hypertensionlung
HM04088EDEM2lymphMESH:D006973Hypertensionheart
HM04088EDEM2lymphMESH:D006973Hypertensionblood vessel
HM04088EDEM2lymphMESH:D005885Gingival Hyperplasia
HM04088EDEM2lymphMESH:D056486Drug-Induced Liver Injury
HM04088EDEM2lymphMESH:D014985Xerophthalmiaeye
HM04088EDEM2lymphMESH:D008664Metal Metabolism, Inborn Errorsskin
HM04088EDEM2lymphMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM04088EDEM2lymphMESH:D008664Metal Metabolism, Inborn Errorsliver
HM04088EDEM2lymphMESH:D008664Metal Metabolism, Inborn Errorskidney
HM04088EDEM2lymphMESH:D019310Pseudolymphoma
HM04088EDEM2lymphMESH:D011565Psoriasisskin
HM04088EDEM2lymphMESH:D008881Migraine Disordersbrain
HM04088EDEM2lymphMESH:D005355Fibrosis
HM04088EDEM2lymphMESH:D012640Seizuresmuscle