Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05756USP33tracheaMESH:D001008Anxiety Disorders
HM05756USP33tracheaMESH:D004938Esophageal Neoplasms
HM05756USP33tracheaMESH:D014564Urogenital Abnormalities
HM05756USP33tracheaMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05756USP33tracheaMESH:D019310Pseudolymphoma
HM05756USP33tracheaMESH:D006333Heart Failureheart
HM05756USP33tracheaMESH:D006330Heart Defects, Congenital
HM05756USP33tracheaMESH:D000550Amblyopiabrain
HM05756USP33tracheaMESH:D000550Amblyopiabrain
HM05756USP33tracheaMESH:D008325Mammary Neoplasms, Experimental
HM05756USP33tracheaMESH:D002471Cell Transformation, Neoplastic
HM05756USP33tracheaMESH:D011471Prostatic Neoplasmsprostate
HM05756USP33tracheaMESH:D012559Schizophrenia
HM05756USP33tracheaMESH:D001714Bipolar Disorder
HM05756USP33tracheaMESH:D012640Seizuresmuscle
HM05756USP33tracheaMESH:D003092Colitis
HM05756USP33tracheaMESH:D013226Status Epilepticusmuscle
HM05756USP33tracheaMESH:D013226Status Epilepticusmuscle
HM05756USP33tracheaMESH:D013226Status Epilepticusmuscle
HM05756USP33tracheaMESH:D010954Plasmacytoma
HM05756USP33tracheaMESH:D000015Abnormalities, Multiple
HM05756USP33tracheaMESH:D006548Hernia, Diaphragmatic
HM05756USP33tracheaMESH:D017029Epilepsy, Complex Partialmuscle
HM05756USP33tracheaMESH:D007676Kidney Failure, Chronickidney
HM05756USP33tracheaMESH:D009190Myelodysplastic Syndromes
HM05756USP33tracheaMESH:D008106Liver Cirrhosis, Experimental
HM05756USP33tracheaMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05756USP33tracheaMESH:D004827Epilepsymuscle
HM05756USP33tracheaMESH:D019247HIV Wasting Syndrome
HM05756USP33tracheaMESH:D001321Autistic Disorder
HM05756USP33tracheaMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05756USP33tracheaMESH:D017563Lung Diseases, Interstitiallung
HM05756USP33tracheaMESH:D000014Abnormalities, Drug-Induced
HM05756USP33tracheaMESH:D012208Rhabdomyosarcomarectum
HM05756USP33tracheaMESH:D012208Rhabdomyosarcomaprostate
HM05756USP33tracheaMESH:D012208Rhabdomyosarcomamuscle
HM05756USP33tracheaMESH:D009436Neural Tube Defects
HM05756USP33tracheaMESH:D009139Musculoskeletal Abnormalities
HM05756USP33tracheaMESH:D008881Migraine Disordersbrain
HM05756USP33tracheaMESH:D005234Fatty Liver
HM05756USP33tracheaMESH:D007674Kidney Diseasesureter
HM05756USP33tracheaMESH:D007674Kidney Diseasespituitary
HM05756USP33tracheaMESH:D007674Kidney Diseaseskidney
HM05756USP33tracheaMESH:D056486Drug-Induced Liver Injury
HM05756USP33tracheaMESH:D006849Hydrocephalusbrain
HM05756USP33tracheaMESH:D008175Lung Neoplasmslung
HM05756USP33tracheaMESH:D001848Bone Diseases, Developmental
HM05756USP33tracheaMESH:D005315Fetal Diseases
HM05756USP33tracheaMESH:D004831Epilepsies, Myoclonicmuscle
HM05756USP33tracheaMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM05756USP33tracheaMESH:D019465Craniofacial Abnormalities
HM05756USP33tracheaMESH:D004421Dystonia
HM05756USP33tracheaMESH:D016135Spinal Dysraphismspinal cord
HM05756USP33tracheaMESH:D020521Strokeblood vessel
HM05756USP33tracheaMESH:D004828Epilepsies, Partialmuscle
HM05756USP33tracheaMESH:D014178Translocation, Genetic
HM05756USP33tracheaMESH:D005317Fetal Growth Retardation
HM05756USP33tracheaMESH:D004832Epilepsy, Absencemuscle
HM05756USP33tracheaMESH:D008654Mesotheliomabone
HM05756USP33tracheaMESH:D002252Carbon Tetrachloride Poisoning
HM05756USP33tracheaMESH:D019584Hot Flashes
HM05756USP33tracheaMESH:D007251Influenza, Human
HM05756USP33tracheaMESH:D008171Lung Diseases