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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03059SHDnerveMESH:D001321Autistic Disorder
HM03059SHDnerveMESH:D004828Epilepsies, Partialmuscle
HM03059SHDnerveMESH:D009436Neural Tube Defects
HM03059SHDnerveMESH:D000550Amblyopiabrain
HM03059SHDnerveMESH:D000550Amblyopiabrain
HM03059SHDnerveMESH:D005234Fatty Liver
HM03059SHDnerveMESH:D009765Obesity
HM03059SHDnerveMESH:D017029Epilepsy, Complex Partialmuscle
HM03059SHDnerveMESH:D017563Lung Diseases, Interstitiallung
HM03059SHDnerveMESH:D015428Myocardial Reperfusion Injury
HM03059SHDnerveMESH:D020194Unverricht-Lundborg Syndromemuscle
HM03059SHDnerveMESH:D006943Hyperglycemia
HM03059SHDnerveMESH:D004421Dystonia
HM03059SHDnerveMESH:D008106Liver Cirrhosis, Experimental
HM03059SHDnerveMESH:D004831Epilepsies, Myoclonicmuscle
HM03059SHDnerveMESH:D016135Spinal Dysraphismspinal cord
HM03059SHDnerveMESH:D004832Epilepsy, Absencemuscle
HM03059SHDnerveMESH:D004487Edema
HM03059SHDnerveMESH:D019310Pseudolymphoma
HM03059SHDnerveMESH:D008113Liver Neoplasms
HM03059SHDnerveMESH:D008113Liver Neoplasms
HM03059SHDnerveMESH:D006849Hydrocephalusbrain
HM03059SHDnerveMESH:D008881Migraine Disordersbrain
HM03059SHDnerveMESH:D014178Translocation, Genetic
HM03059SHDnerveMESH:D055371Acute Lung Injury
HM03059SHDnerveMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM03059SHDnerveMESH:D009203Myocardial Infarctionheart
HM03059SHDnerveMESH:D000014Abnormalities, Drug-Induced
HM03059SHDnerveMESH:D018248Adenoma, Liver Cell
HM03059SHDnerveMESH:D001848Bone Diseases, Developmental
HM03059SHDnerveMESH:D009190Myelodysplastic Syndromes
HM03059SHDnerveMESH:D006529Hepatomegaly
HM03059SHDnerveMESH:D009369Neoplasmsspleen
HM03059SHDnerveMESH:D009369Neoplasmsbone marrow
HM03059SHDnerveMESH:D015427Reperfusion Injury
HM03059SHDnerveMESH:D012208Rhabdomyosarcomarectum
HM03059SHDnerveMESH:D012208Rhabdomyosarcomaprostate
HM03059SHDnerveMESH:D012208Rhabdomyosarcomamuscle
HM03059SHDnerveMESH:D056486Drug-Induced Liver Injury
HM03059SHDnerveMESH:D000015Abnormalities, Multiple
HM03059SHDnerveMESH:D006333Heart Failureheart
HM03059SHDnerveMESH:D007333Insulin Resistance
HM03059SHDnerveMESH:D019465Craniofacial Abnormalities
HM03059SHDnerveMESH:D001008Anxiety Disorders
HM03059SHDnerveMESH:D013226Status Epilepticusmuscle
HM03059SHDnerveMESH:D013226Status Epilepticusmuscle
HM03059SHDnerveMESH:D013226Status Epilepticusmuscle
HM03059SHDnerveMESH:D001714Bipolar Disorder
HM03059SHDnerveMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM03059SHDnerveMESH:D004827Epilepsymuscle
HM03059SHDnerveMESH:D012559Schizophrenia
HM03059SHDnerveMESH:D003876Dermatitis, Atopicskin
HM03059SHDnerveMESH:D012640Seizuresmuscle
HM03059SHDnerveMESH:D014564Urogenital Abnormalities
HM03059SHDnerveMESH:D005317Fetal Growth Retardation
HM03059SHDnerveMESH:D009135Muscular Diseasesmuscle
HM03059SHDnerveMESH:D005315Fetal Diseases
HM03059SHDnerveMESH:D002779Cholestasisliver
HM03059SHDnerveMESH:D009139Musculoskeletal Abnormalities
HM03059SHDnerveMESH:D001778Blood Coagulation Disordersbone marrow