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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05687ZNF227thymusMESH:D006849Hydrocephalusbrain
HM05687ZNF227thymusMESH:D005885Gingival Hyperplasia
HM05687ZNF227thymusMESH:D009436Neural Tube Defects
HM05687ZNF227thymusMESH:D019310Pseudolymphoma
HM05687ZNF227thymusMESH:D056486Drug-Induced Liver Injury
HM05687ZNF227thymusMESH:D005317Fetal Growth Retardation
HM05687ZNF227thymusMESH:D012208Rhabdomyosarcomarectum
HM05687ZNF227thymusMESH:D012208Rhabdomyosarcomaprostate
HM05687ZNF227thymusMESH:D012208Rhabdomyosarcomamuscle
HM05687ZNF227thymusMESH:D009402Nephrosis, Lipoidkidney
HM05687ZNF227thymusMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05687ZNF227thymusMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05687ZNF227thymusMESH:D017563Lung Diseases, Interstitiallung
HM05687ZNF227thymusMESH:D005234Fatty Liver
HM05687ZNF227thymusMESH:D009139Musculoskeletal Abnormalities
HM05687ZNF227thymusMESH:D001008Anxiety Disorders
HM05687ZNF227thymusMESH:D014178Translocation, Genetic
HM05687ZNF227thymusMESH:D004831Epilepsies, Myoclonicmuscle
HM05687ZNF227thymusMESH:D004827Epilepsymuscle
HM05687ZNF227thymusMESH:D004832Epilepsy, Absencemuscle
HM05687ZNF227thymusMESH:D008881Migraine Disordersbrain
HM05687ZNF227thymusMESH:D016135Spinal Dysraphismspinal cord
HM05687ZNF227thymusMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05687ZNF227thymusMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05687ZNF227thymusMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05687ZNF227thymusMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05687ZNF227thymusMESH:D012559Schizophrenia
HM05687ZNF227thymusMESH:D012640Seizuresmuscle
HM05687ZNF227thymusMESH:D000014Abnormalities, Drug-Induced
HM05687ZNF227thymusMESH:D019465Craniofacial Abnormalities
HM05687ZNF227thymusMESH:D007638Keratoconjunctivitis Siccaeye
HM05687ZNF227thymusMESH:D005315Fetal Diseases
HM05687ZNF227thymusMESH:D006973Hypertensionlung
HM05687ZNF227thymusMESH:D006973Hypertensionheart
HM05687ZNF227thymusMESH:D006973Hypertensionblood vessel
HM05687ZNF227thymusMESH:D014564Urogenital Abnormalities
HM05687ZNF227thymusMESH:D000015Abnormalities, Multiple
HM05687ZNF227thymusMESH:D012878Skin Neoplasms
HM05687ZNF227thymusMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05687ZNF227thymusMESH:D013226Status Epilepticusmuscle
HM05687ZNF227thymusMESH:D013226Status Epilepticusmuscle
HM05687ZNF227thymusMESH:D013226Status Epilepticusmuscle
HM05687ZNF227thymusMESH:D000550Amblyopiabrain
HM05687ZNF227thymusMESH:D000550Amblyopiabrain
HM05687ZNF227thymusMESH:D017029Epilepsy, Complex Partialmuscle
HM05687ZNF227thymusMESH:D009404Nephrotic Syndromekidney
HM05687ZNF227thymusMESH:D014605Uveitiseye
HM05687ZNF227thymusMESH:D004828Epilepsies, Partialmuscle
HM05687ZNF227thymusMESH:D001848Bone Diseases, Developmental
HM05687ZNF227thymusMESH:D007674Kidney Diseasesureter
HM05687ZNF227thymusMESH:D007674Kidney Diseasespituitary
HM05687ZNF227thymusMESH:D007674Kidney Diseaseskidney
HM05687ZNF227thymusMESH:D009190Myelodysplastic Syndromes
HM05687ZNF227thymusMESH:D001714Bipolar Disorder
HM05687ZNF227thymusMESH:D004421Dystonia
HM05687ZNF227thymusMESH:D005355Fibrosis
HM05687ZNF227thymusMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM05687ZNF227thymusMESH:D001321Autistic Disorder
HM05687ZNF227thymusMESH:D011565Psoriasisskin
HM05687ZNF227thymusMESH:D014985Xerophthalmiaeye
HM05687ZNF227thymusMESH:D006457Hemoglobinuria, Paroxysmal