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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06891PGAM2heartMESH:D008113Liver Neoplasms
HM06891PGAM2heartMESH:D008113Liver Neoplasms
HM06891PGAM2heartMESH:D006869Hydronephrosiskidney
HM06891PGAM2heartMESH:D001836Body Weight Changes
HM06891PGAM2heartMESH:D006470Hemorrhage
HM06891PGAM2heartMESH:D020246Venous Thrombosis
HM06891PGAM2heartMESH:D001321Autistic Disorder
HM06891PGAM2heartMESH:D005315Fetal Diseases
HM06891PGAM2heartMESH:D019966Substance-Related Disorders
HM06891PGAM2heartMESH:D006330Heart Defects, Congenital
HM06891PGAM2heartMESH:D019851Thrombophiliabone marrow
HM06891PGAM2heartMESH:D003924Diabetes Mellitus, Type 2pancreas
HM06891PGAM2heartMESH:D013927Thrombosis
HM06891PGAM2heartMESH:D020194Unverricht-Lundborg Syndromemuscle
HM06891PGAM2heartMESH:D001943Breast Neoplasmsbreast
HM06891PGAM2heartMESH:D008175Lung Neoplasmslung
HM06891PGAM2heartMESH:D008881Migraine Disordersbrain
HM06891PGAM2heartMESH:D005317Fetal Growth Retardation
HM06891PGAM2heartMESH:D007569Jaw Abnormalities
HM06891PGAM2heartMESH:D001778Blood Coagulation Disordersbone marrow
HM06891PGAM2heartMESH:D004489Edema, Cardiac
HM06891PGAM2heartOMIM:261670GLYCOGEN STORAGE DISEASE X
HM06891PGAM2heartMESH:D006973Hypertensionlung
HM06891PGAM2heartMESH:D006973Hypertensionheart
HM06891PGAM2heartMESH:D006973Hypertensionblood vessel
HM06891PGAM2heartMESH:D000152Acne Vulgaris
HM06891PGAM2heartMESH:D007333Insulin Resistance
HM06891PGAM2heartMESH:D004828Epilepsies, Partialmuscle
HM06891PGAM2heartMESH:D005313Fetal Death
HM06891PGAM2heartMESH:D002278Carcinoma in Situ
HM06891PGAM2heartMESH:D002278Carcinoma in Situ
HM06891PGAM2heartMESH:D000013Congenital Abnormalities
HM06891PGAM2heartMESH:D007248Infertility, Male
HM06891PGAM2heartMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM06891PGAM2heartMESH:D013226Status Epilepticusmuscle
HM06891PGAM2heartMESH:D013226Status Epilepticusmuscle
HM06891PGAM2heartMESH:D013226Status Epilepticusmuscle
HM06891PGAM2heartMESH:D014594Uterine Neoplasmscervix
HM06891PGAM2heartMESH:D014594Uterine Neoplasms
HM06891PGAM2heartMESH:D054079Vascular Malformations
HM06891PGAM2heartMESH:D005355Fibrosis
HM06891PGAM2heartMESH:D012640Seizuresmuscle
HM06891PGAM2heartMESH:D013088Spermatocele
HM06891PGAM2heartMESH:D018281Cholangiocarcinomaliver
HM06891PGAM2heartMESH:D004832Epilepsy, Absencemuscle
HM06891PGAM2heartMESH:D009139Musculoskeletal Abnormalities
HM06891PGAM2heartMESH:D010049Ovarian Diseasesovary
HM06891PGAM2heartMESH:D012208Rhabdomyosarcomarectum
HM06891PGAM2heartMESH:D012208Rhabdomyosarcomaprostate
HM06891PGAM2heartMESH:D012208Rhabdomyosarcomamuscle
HM06891PGAM2heartMESH:D016135Spinal Dysraphismspinal cord
HM06891PGAM2heartMESH:D005234Fatty Liver
HM06891PGAM2heartMESH:D007021Hypospadias
HM06891PGAM2heartMESH:D001008Anxiety Disorders
HM06891PGAM2heartMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM06891PGAM2heartMESH:D000230Adenocarcinoma
HM06891PGAM2heartMESH:D000230Adenocarcinomauterus
HM06891PGAM2heartMESH:D000230Adenocarcinoma
HM06891PGAM2heartMESH:D000230Adenocarcinoma
HM06891PGAM2heartMESH:D000230Adenocarcinomauterus
HM06891PGAM2heartMESH:D000230Adenocarcinomathyroid
HM06891PGAM2heartMESH:D000230Adenocarcinomaskin
HM06891PGAM2heartMESH:D000230Adenocarcinomaparathyroid gland
HM06891PGAM2heartMESH:D000230Adenocarcinomaliver
HM06891PGAM2heartMESH:D000230Adenocarcinomakidney
HM06891PGAM2heartMESH:D000230Adenocarcinomaeye
HM06891PGAM2heartMESH:D000230Adenocarcinomaadrenal gland
HM06891PGAM2heartMESH:D000740Anemiabone marrow
HM06891PGAM2heartMESH:D056486Drug-Induced Liver Injury
HM06891PGAM2heartMESH:D011297Prenatal Exposure Delayed Effects
HM06891PGAM2heartMESH:D012559Schizophrenia
HM06891PGAM2heartMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM06891PGAM2heartMESH:D017202Myocardial Ischemiaheart
HM06891PGAM2heartMESH:D001862Bone Resorption
HM06891PGAM2heartMESH:D005124Eye Abnormalities
HM06891PGAM2heartMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM06891PGAM2heartMESH:D007249Inflammation
HM06891PGAM2heartMESH:D017563Lung Diseases, Interstitiallung
HM06891PGAM2heartMESH:D015619Respiratory System Abnormalities
HM06891PGAM2heartMESH:D013959Thyroid Diseasesthyroid
HM06891PGAM2heartMESH:D004421Dystonia
HM06891PGAM2heartMESH:D004827Epilepsymuscle
HM06891PGAM2heartMESH:D002972Cleft Palate
HM06891PGAM2heartMESH:D007247Infertility, Female
HM06891PGAM2heartMESH:D008106Liver Cirrhosis, Experimental
HM06891PGAM2heartMESH:D000014Abnormalities, Drug-Induced
HM06891PGAM2heartMESH:D006332Cardiomegaly
HM06891PGAM2heartMESH:D006849Hydrocephalusbrain
HM06891PGAM2heartMESH:D001161Arteriosclerosisblood vessel
HM06891PGAM2heartMESH:D001169Arthritis, Experimental
HM06891PGAM2heartMESH:D002277Carcinoma
HM06891PGAM2heartMESH:D019282Wasting Syndrome
HM06891PGAM2heartMESH:D000015Abnormalities, Multiple
HM06891PGAM2heartMESH:D018248Adenoma, Liver Cell
HM06891PGAM2heartMESH:D017119Porphyria Cutanea Tardaskin
HM06891PGAM2heartMESH:D017029Epilepsy, Complex Partialmuscle
HM06891PGAM2heartMESH:D011537Pruritus
HM06891PGAM2heartMESH:D009436Neural Tube Defects
HM06891PGAM2heartMESH:D010382Peliosis Hepatisliver
HM06891PGAM2heartMESH:D012878Skin Neoplasms
HM06891PGAM2heartMESH:D014591Uterine Diseasesuterus
HM06891PGAM2heartMESH:D014591Uterine Diseasesplacenta
HM06891PGAM2heartMESH:D014591Uterine Diseasescervix
HM06891PGAM2heartMESH:D004362Drug Toxicity
HM06891PGAM2heartMESH:D004831Epilepsies, Myoclonicmuscle
HM06891PGAM2heartMESH:D002779Cholestasisliver
HM06891PGAM2heartMESH:D014564Urogenital Abnormalities
HM06891PGAM2heartMESH:D016584Panic Disorder
HM06891PGAM2heartMESH:D011471Prostatic Neoplasmsprostate
HM06891PGAM2heartMESH:D006529Hepatomegaly
HM06891PGAM2heartMESH:D019465Craniofacial Abnormalities
HM06891PGAM2heartMESH:D009421Nervous System Malformations
HM06891PGAM2heartMESH:D000550Amblyopiabrain
HM06891PGAM2heartMESH:D000550Amblyopiabrain
HM06891PGAM2heartMESH:D001714Bipolar Disorder
HM06891PGAM2heartMESH:D001848Bone Diseases, Developmental
HM06891PGAM2heartMESH:D009190Myelodysplastic Syndromes
HM06891PGAM2heartMESH:D008114Liver Neoplasms, Experimental
HM06891PGAM2heartMESH:D004487Edema
HM06891PGAM2heartMESH:D011629Puberty, Precocious
HM06891PGAM2heartMESH:D014178Translocation, Genetic
HM06891PGAM2heartMESH:D019310Pseudolymphoma