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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04642SPASTthyroidMESH:D001848Bone Diseases, Developmental
HM04642SPASTthyroidMESH:D009369Neoplasmsspleen
HM04642SPASTthyroidMESH:D009369Neoplasmsbone marrow
HM04642SPASTthyroidMESH:D056486Drug-Induced Liver Injury
HM04642SPASTthyroidMESH:D011014Pneumonialung
HM04642SPASTthyroidMESH:D008113Liver Neoplasms
HM04642SPASTthyroidMESH:D008113Liver Neoplasms
HM04642SPASTthyroidMESH:D006470Hemorrhage
HM04642SPASTthyroidMESH:D002583Uterine Cervical Neoplasmscervix
HM04642SPASTthyroidMESH:D006330Heart Defects, Congenital
HM04642SPASTthyroidMESH:D017202Myocardial Ischemiaheart
HM04642SPASTthyroidMESH:D016535Bronchial Hyperreactivity
HM04642SPASTthyroidMESH:D002100Cachexia
HM04642SPASTthyroidMESH:D011297Prenatal Exposure Delayed Effects
HM04642SPASTthyroidMESH:D002277Carcinoma
HM04642SPASTthyroidMESH:D010911Pituitary Neoplasms
HM04642SPASTthyroidMESH:D010911Pituitary Neoplasmspituitary
HM04642SPASTthyroidMESH:D010911Pituitary Neoplasmspituitary
HM04642SPASTthyroidMESH:D004714Endometrial Hyperplasia
HM04642SPASTthyroidMESH:D000544Alzheimer Diseasenerve
HM04642SPASTthyroidMESH:D006332Cardiomegaly
HM04642SPASTthyroidMESH:D052776Female Urogenital Diseases
HM04642SPASTthyroidMESH:D007021Hypospadias
HM04642SPASTthyroidMESH:D008171Lung Diseases
HM04642SPASTthyroidMESH:D009421Nervous System Malformations
HM04642SPASTthyroidMESH:D008181Lupus Nephritis
HM04642SPASTthyroidMESH:D010900Pituitary Diseasespituitary
HM04642SPASTthyroidMESH:D018281Cholangiocarcinomaliver
HM04642SPASTthyroidMESH:D005124Eye Abnormalities
HM04642SPASTthyroidMESH:D018248Adenoma, Liver Cell
HM04642SPASTthyroidMESH:D007249Inflammation
HM04642SPASTthyroidMESH:D001321Autistic Disorder
HM04642SPASTthyroidMESH:D013959Thyroid Diseasesthyroid
HM04642SPASTthyroidMESH:D001172Arthritis, Rheumatoidbone
HM04642SPASTthyroidMESH:D004487Edema
HM04642SPASTthyroidMESH:D004489Edema, Cardiac
HM04642SPASTthyroidMESH:D005355Fibrosis
HM04642SPASTthyroidMESH:D019465Craniofacial Abnormalities
HM04642SPASTthyroidMESH:D006529Hepatomegaly
HM04642SPASTthyroidMESH:D003924Diabetes Mellitus, Type 2pancreas
HM04642SPASTthyroidMESH:D001249Asthmalung
HM04642SPASTthyroidMESH:D005313Fetal Death
HM04642SPASTthyroidMESH:D014594Uterine Neoplasmscervix
HM04642SPASTthyroidMESH:D014594Uterine Neoplasms
HM04642SPASTthyroidMESH:D010538Peritonitis
HM04642SPASTthyroidMESH:D015619Respiratory System Abnormalities
HM04642SPASTthyroidMESH:D014625Vaginal Neoplasmsbone
HM04642SPASTthyroidMESH:D014625Vaginal Neoplasms
HM04642SPASTthyroidMESH:D006973Hypertensionlung
HM04642SPASTthyroidMESH:D006973Hypertensionheart
HM04642SPASTthyroidMESH:D006973Hypertensionblood vessel
HM04642SPASTthyroidMESH:D014591Uterine Diseasesuterus
HM04642SPASTthyroidMESH:D014591Uterine Diseasesplacenta
HM04642SPASTthyroidMESH:D014591Uterine Diseasescervix
HM04642SPASTthyroidMESH:D054079Vascular Malformations
HM04642SPASTthyroidMESH:D006869Hydronephrosiskidney
HM04642SPASTthyroidMESH:D016889Endometrial Neoplasmsuterus
HM04642SPASTthyroidMESH:D012878Skin Neoplasms
HM04642SPASTthyroidMESH:D001749Urinary Bladder Neoplasmsureter
HM04642SPASTthyroidMESH:D001749Urinary Bladder Neoplasmsbladder
HM04642SPASTthyroidMESH:D052801Male Urogenital Diseases
HM04642SPASTthyroidMESH:D005833Genital Neoplasms, Female
HM04642SPASTthyroidMESH:D000686Amyloidosis
HM04642SPASTthyroidMESH:D001836Body Weight Changes
HM04642SPASTthyroidMESH:D006528Carcinoma, Hepatocellularliver
HM04642SPASTthyroidMESH:D007569Jaw Abnormalities
HM04642SPASTthyroidMESH:D007859Learning Disorders
HM04642SPASTthyroidMESH:D010382Peliosis Hepatisliver
HM04642SPASTthyroidMESH:D000014Abnormalities, Drug-Induced
HM04642SPASTthyroidMESH:D008679Metaplasia
HM04642SPASTthyroidMESH:D008223Lymphoma
HM04642SPASTthyroidMESH:D005334Fever
HM04642SPASTthyroidMESH:D007680Kidney Neoplasmskidney
HM04642SPASTthyroidMESH:D001778Blood Coagulation Disordersbone marrow
HM04642SPASTthyroidMESH:D019282Wasting Syndrome
HM04642SPASTthyroidMESH:D008114Liver Neoplasms, Experimental
HM04642SPASTthyroidMESH:D008106Liver Cirrhosis, Experimental
HM04642SPASTthyroidMESH:D002972Cleft Palate
HM04642SPASTthyroidMESH:D006965Hyperplasia
HM04642SPASTthyroidMESH:D007246Infertility
HM04642SPASTthyroidMESH:D000740Anemiabone marrow
HM04642SPASTthyroidMESH:D003456Cryptorchidism
HM04642SPASTthyroidMESH:D008175Lung Neoplasmslung
HM04642SPASTthyroidMESH:D001943Breast Neoplasmsbreast
HM04642SPASTthyroidMESH:D017119Porphyria Cutanea Tardaskin
HM04642SPASTthyroidMESH:D004362Drug Toxicity
HM04642SPASTthyroidMESH:D013088Spermatocele
HM04642SPASTthyroidMESH:D000013Congenital Abnormalities
HM04642SPASTthyroidMESH:D011471Prostatic Neoplasmsprostate
HM04642SPASTthyroidMESH:C536865Spastic paraplegia 4, autosomal dominant