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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06477DGCR5kidneyMESH:D008881Migraine Disordersbrain
HM06477DGCR5kidneyMESH:D014564Urogenital Abnormalities
HM06477DGCR5kidneyMESH:D000014Abnormalities, Drug-Induced
HM06477DGCR5kidneyMESH:D012559Schizophrenia
HM06477DGCR5kidneyMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06477DGCR5kidneyMESH:D005317Fetal Growth Retardation
HM06477DGCR5kidneyMESH:D005234Fatty Liver
HM06477DGCR5kidneyMESH:D004832Epilepsy, Absencemuscle
HM06477DGCR5kidneyMESH:D017029Epilepsy, Complex Partialmuscle
HM06477DGCR5kidneyMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06477DGCR5kidneyMESH:D012208Rhabdomyosarcomarectum
HM06477DGCR5kidneyMESH:D012208Rhabdomyosarcomaprostate
HM06477DGCR5kidneyMESH:D012208Rhabdomyosarcomamuscle
HM06477DGCR5kidneyMESH:D000550Amblyopiabrain
HM06477DGCR5kidneyMESH:D000550Amblyopiabrain
HM06477DGCR5kidneyMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM06477DGCR5kidneyMESH:D004831Epilepsies, Myoclonicmuscle
HM06477DGCR5kidneyMESH:D001008Anxiety Disorders
HM06477DGCR5kidneyMESH:D009190Myelodysplastic Syndromes
HM06477DGCR5kidneyMESH:D012640Seizuresmuscle
HM06477DGCR5kidneyMESH:D001714Bipolar Disorder
HM06477DGCR5kidneyMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06477DGCR5kidneyMESH:D001321Autistic Disorder
HM06477DGCR5kidneyMESH:D019465Craniofacial Abnormalities
HM06477DGCR5kidneyMESH:D019310Pseudolymphoma
HM06477DGCR5kidneyMESH:D009436Neural Tube Defects
HM06477DGCR5kidneyMESH:D004421Dystonia
HM06477DGCR5kidneyMESH:D017563Lung Diseases, Interstitiallung
HM06477DGCR5kidneyMESH:D009139Musculoskeletal Abnormalities
HM06477DGCR5kidneyMESH:D006849Hydrocephalusbrain
HM06477DGCR5kidneyMESH:D005315Fetal Diseases
HM06477DGCR5kidneyMESH:D013226Status Epilepticusmuscle
HM06477DGCR5kidneyMESH:D013226Status Epilepticusmuscle
HM06477DGCR5kidneyMESH:D013226Status Epilepticusmuscle
HM06477DGCR5kidneyMESH:D004828Epilepsies, Partialmuscle
HM06477DGCR5kidneyMESH:D016135Spinal Dysraphismspinal cord
HM06477DGCR5kidneyMESH:D014178Translocation, Genetic
HM06477DGCR5kidneyMESH:D000015Abnormalities, Multiple
HM06477DGCR5kidneyMESH:D001848Bone Diseases, Developmental
HM06477DGCR5kidneyMESH:D004827Epilepsymuscle
HM06477DGCR5kidneyMESH:D056486Drug-Induced Liver Injury