Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06413MMP17skinMESH:D017202Myocardial Ischemiaheart
HM06413MMP17skinMESH:D012208Rhabdomyosarcomarectum
HM06413MMP17skinMESH:D012208Rhabdomyosarcomaprostate
HM06413MMP17skinMESH:D012208Rhabdomyosarcomamuscle
HM06413MMP17skinMESH:D001778Blood Coagulation Disordersbone marrow
HM06413MMP17skinMESH:D004827Epilepsymuscle
HM06413MMP17skinMESH:D009421Nervous System Malformations
HM06413MMP17skinMESH:D019465Craniofacial Abnormalities
HM06413MMP17skinMESH:D019310Pseudolymphoma
HM06413MMP17skinMESH:D005234Fatty Liver
HM06413MMP17skinMESH:D005313Fetal Death
HM06413MMP17skinMESH:D006849Hydrocephalusbrain
HM06413MMP17skinMESH:D008113Liver Neoplasms
HM06413MMP17skinMESH:D008113Liver Neoplasms
HM06413MMP17skinMESH:D009436Neural Tube Defects
HM06413MMP17skinMESH:D019282Wasting Syndrome
HM06413MMP17skinMESH:D007569Jaw Abnormalities
HM06413MMP17skinMESH:D000740Anemiabone marrow
HM06413MMP17skinMESH:D004421Dystonia
HM06413MMP17skinMESH:D004828Epilepsies, Partialmuscle
HM06413MMP17skinMESH:D018248Adenoma, Liver Cell
HM06413MMP17skinMESH:D008107Liver Diseasesskin
HM06413MMP17skinMESH:D008107Liver Diseasesmuscle
HM06413MMP17skinMESH:D008107Liver Diseaseslung
HM06413MMP17skinMESH:D008107Liver Diseasesliver
HM06413MMP17skinMESH:D011471Prostatic Neoplasmsprostate
HM06413MMP17skinMESH:D017029Epilepsy, Complex Partialmuscle
HM06413MMP17skinMESH:D009190Myelodysplastic Syndromes
HM06413MMP17skinMESH:D000013Congenital Abnormalities
HM06413MMP17skinMESH:D004831Epilepsies, Myoclonicmuscle
HM06413MMP17skinMESH:D006529Hepatomegaly
HM06413MMP17skinMESH:D013959Thyroid Diseasesthyroid
HM06413MMP17skinMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06413MMP17skinMESH:D003924Diabetes Mellitus, Type 2pancreas
HM06413MMP17skinMESH:D004362Drug Toxicity
HM06413MMP17skinMESH:D004489Edema, Cardiac
HM06413MMP17skinMESH:D013226Status Epilepticusmuscle
HM06413MMP17skinMESH:D013226Status Epilepticusmuscle
HM06413MMP17skinMESH:D013226Status Epilepticusmuscle
HM06413MMP17skinMESH:D010382Peliosis Hepatisliver
HM06413MMP17skinMESH:D019457Chromosome Breakage
HM06413MMP17skinMESH:D004832Epilepsy, Absencemuscle
HM06413MMP17skinMESH:D012559Schizophrenia
HM06413MMP17skinMESH:D001714Bipolar Disorder
HM06413MMP17skinMESH:D000550Amblyopiabrain
HM06413MMP17skinMESH:D000550Amblyopiabrain
HM06413MMP17skinMESH:D006932Hyperbilirubinemia
HM06413MMP17skinMESH:D015619Respiratory System Abnormalities
HM06413MMP17skinMESH:D001836Body Weight Changes
HM06413MMP17skinMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06413MMP17skinMESH:D014564Urogenital Abnormalities
HM06413MMP17skinMESH:D014178Translocation, Genetic
HM06413MMP17skinMESH:D054079Vascular Malformations
HM06413MMP17skinMESH:D012640Seizuresmuscle
HM06413MMP17skinMESH:D007249Inflammation
HM06413MMP17skinMESH:D008881Migraine Disordersbrain
HM06413MMP17skinMESH:D006869Hydronephrosiskidney
HM06413MMP17skinMESH:D012878Skin Neoplasms
HM06413MMP17skinMESH:D011297Prenatal Exposure Delayed Effects
HM06413MMP17skinMESH:D008103Liver Cirrhosisliver
HM06413MMP17skinMESH:D016393Lymphoma, B-Cell
HM06413MMP17skinMESH:D017093Liver Failure
HM06413MMP17skinMESH:D017563Lung Diseases, Interstitiallung
HM06413MMP17skinMESH:D001848Bone Diseases, Developmental
HM06413MMP17skinMESH:D001321Autistic Disorder
HM06413MMP17skinMESH:D000015Abnormalities, Multiple
HM06413MMP17skinMESH:D008106Liver Cirrhosis, Experimental
HM06413MMP17skinMESH:D003920Diabetes Mellituspancreas
HM06413MMP17skinMESH:D056486Drug-Induced Liver Injury
HM06413MMP17skinMESH:D007333Insulin Resistance
HM06413MMP17skinMESH:D004487Edema
HM06413MMP17skinMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06413MMP17skinMESH:D000014Abnormalities, Drug-Induced
HM06413MMP17skinMESH:D008175Lung Neoplasmslung
HM06413MMP17skinMESH:D001943Breast Neoplasmsbreast
HM06413MMP17skinMESH:D009139Musculoskeletal Abnormalities
HM06413MMP17skinMESH:D018281Cholangiocarcinomaliver
HM06413MMP17skinMESH:D017119Porphyria Cutanea Tardaskin
HM06413MMP17skinMESH:D005315Fetal Diseases
HM06413MMP17skinMESH:D005355Fibrosis
HM06413MMP17skinMESH:D016135Spinal Dysraphismspinal cord
HM06413MMP17skinMESH:D002972Cleft Palate
HM06413MMP17skinMESH:D006470Hemorrhage
HM06413MMP17skinMESH:D017114Liver Failure, Acute
HM06413MMP17skinMESH:D001008Anxiety Disorders
HM06413MMP17skinMESH:D006332Cardiomegaly
HM06413MMP17skinMESH:D005124Eye Abnormalities
HM06413MMP17skinMESH:D005317Fetal Growth Retardation
HM06413MMP17skinMESH:D006330Heart Defects, Congenital
HM06413MMP17skinMESH:D006973Hypertensionlung
HM06413MMP17skinMESH:D006973Hypertensionheart
HM06413MMP17skinMESH:D006973Hypertensionblood vessel
HM06413MMP17skinMESH:D008114Liver Neoplasms, Experimental
HM06413MMP17skinMESH:D002252Carbon Tetrachloride Poisoning
HM06413MMP17skinMESH:D002277Carcinoma
HM06413MMP17skinMESH:D006505Hepatitis