Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00001SFTPClungMESH:D000686Amyloidosis
HM00001SFTPClungMESH:D010190Pancreatic Neoplasmspancreas
HM00001SFTPClungMESH:D018290Cervical Intraepithelial Neoplasia
HM00001SFTPClungMESH:D014062Tongue Neoplasms
HM00001SFTPClungMESH:D004362Drug Toxicity
HM00001SFTPClungMESH:D016889Endometrial Neoplasmsuterus
HM00001SFTPClungMESH:D006529Hepatomegaly
HM00001SFTPClungMESH:D007951Leukemia, Myeloidbone marrow
HM00001SFTPClungMESH:D008108Liver Diseases, Alcoholic
HM00001SFTPClungMESH:D011654Pulmonary Edemalung
HM00001SFTPClungMESH:D054079Vascular Malformations
HM00001SFTPClungMESH:D018236Carcinoma, Embryonal
HM00001SFTPClungMESH:D003922Diabetes Mellitus, Type 1pancreas
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmsthyroid
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmsskin
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmslarynx
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmsear
HM00001SFTPClungMESH:D006258Head and Neck Neoplasmsbrain
HM00001SFTPClungMESH:D006869Hydronephrosiskidney
HM00001SFTPClungMESH:D000505Alopeciaskin
HM00001SFTPClungMESH:D006986Hypervitaminosis A
HM00001SFTPClungMESH:D013959Thyroid Diseasesthyroid
HM00001SFTPClungMESH:D005909Glioblastomabone
HM00001SFTPClungMESH:D005909Glioblastomabrain
HM00001SFTPClungMESH:D005909Glioblastomabone
HM00001SFTPClungMESH:D053609Lethargy
HM00001SFTPClungMESH:D011537Pruritus
HM00001SFTPClungMESH:D006976Hypertension, Pulmonarylung
HM00001SFTPClungMESH:D008325Mammary Neoplasms, Experimental
HM00001SFTPClungMESH:D001161Arteriosclerosisblood vessel
HM00001SFTPClungMESH:D002289Carcinoma, Non-Small-Cell Lunglung
HM00001SFTPClungMESH:D019465Craniofacial Abnormalities
HM00001SFTPClungMESH:D000152Acne Vulgaris
HM00001SFTPClungMESH:D009101Multiple Myelomabone marrow
HM00001SFTPClungMESH:D002294Carcinoma, Squamous Celllung
HM00001SFTPClungMESH:D002294Carcinoma, Squamous Cellliver
HM00001SFTPClungMESH:D002294Carcinoma, Squamous Celllarynx
HM00001SFTPClungMESH:D002294Carcinoma, Squamous Cellkidney
HM00001SFTPClungMESH:D002294Carcinoma, Squamous Celleye
HM00001SFTPClungMESH:D008223Lymphoma
HM00001SFTPClungMESH:D019282Wasting Syndrome
HM00001SFTPClungMESH:D001943Breast Neoplasmsbreast
HM00001SFTPClungMESH:D006679HIV Seropositivity
HM00001SFTPClungMESH:D054990Idiopathic Pulmonary Fibrosislung
HM00001SFTPClungMESH:D018798Anemia, Iron-Deficiencybone marrow
HM00001SFTPClungMESH:D010212Papillomabrain
HM00001SFTPClungMESH:D010212Papillomaliver
HM00001SFTPClungMESH:D010212Papilloma
HM00001SFTPClungMESH:D000013Congenital Abnormalities
HM00001SFTPClungMESH:D030342Genetic Diseases, Inborn
HM00001SFTPClungMESH:D006548Hernia, Diaphragmatic
HM00001SFTPClungMESH:D009369Neoplasmsspleen
HM00001SFTPClungMESH:D009369Neoplasmsbone marrow
HM00001SFTPClungMESH:D007752Obstetric Labor, Premature
HM00001SFTPClungMESH:D013272Stomach Diseasesblood vessel
HM00001SFTPClungMESH:D002386Cataractpancreas
HM00001SFTPClungMESH:D002386Cataracteye
HM00001SFTPClungMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM00001SFTPClungMESH:D018248Adenoma, Liver Cell
HM00001SFTPClungMESH:D015362Child Nutrition Disorders
HM00001SFTPClungMESH:D005355Fibrosis
HM00001SFTPClungMESH:D006470Hemorrhage
HM00001SFTPClungMESH:D006930Hyperalgesia
HM00001SFTPClungMESH:D003456Cryptorchidism
HM00001SFTPClungMESH:D006973Hypertensionlung
HM00001SFTPClungMESH:D006973Hypertensionheart
HM00001SFTPClungMESH:D006973Hypertensionblood vessel
HM00001SFTPClungMESH:D008175Lung Neoplasmslung
HM00001SFTPClungMESH:D009190Myelodysplastic Syndromes
HM00001SFTPClungMESH:D001471Barrett Esophagusesophagus
HM00001SFTPClungMESH:D004480Ectromelia
HM00001SFTPClungMESH:D004489Edema, Cardiac
HM00001SFTPClungMESH:D007410Intestinal Diseasessmall intestine
HM00001SFTPClungMESH:D007410Intestinal Diseasesrectum
HM00001SFTPClungMESH:D007410Intestinal Diseasescolon
HM00001SFTPClungMESH:D007410Intestinal Diseasesblood vessel
HM00001SFTPClungMESH:D013964Thyroid Neoplasmsthyroid
HM00001SFTPClungMESH:D009396Wilms Tumorkidney
HM00001SFTPClungMESH:D009396Wilms Tumorcervix
HM00001SFTPClungMESH:D006261Headache
HM00001SFTPClungMESH:D008881Migraine Disordersbrain
HM00001SFTPClungMESH:D012128Respiratory Distress Syndrome, Adultlung
HM00001SFTPClungMESH:D001778Blood Coagulation Disordersbone marrow
HM00001SFTPClungMESH:D005313Fetal Death
HM00001SFTPClungMESH:D015658HIV Infections
HM00001SFTPClungMESH:D011507Proteinuriakidney
HM00001SFTPClungMESH:D002779Cholestasisliver
HM00001SFTPClungMESH:D015473Leukemia, Promyelocytic, Acute
HM00001SFTPClungMESH:D012555Schistosomiasis mansoni
HM00001SFTPClungMESH:D000544Alzheimer Diseasenerve
HM00001SFTPClungMESH:D017449Dermatitis, Allergic Contactskin
HM00001SFTPClungMESH:D008171Lung Diseases
HM00001SFTPClungMESH:D011469Prostatic Diseasesureter
HM00001SFTPClungMESH:D011469Prostatic Diseasesprostate
HM00001SFTPClungMESH:D011658Pulmonary Fibrosislung
HM00001SFTPClungMESH:D017202Myocardial Ischemiaheart
HM00001SFTPClungMESH:D010146Pain
HM00001SFTPClungMESH:D006332Cardiomegaly
HM00001SFTPClungMESH:D002972Cleft Palate
HM00001SFTPClungOMIM:610913SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2
HM00001SFTPClungMESH:D014820Vitiligobone marrow
HM00001SFTPClungMESH:D005327Fetal Resorption
HM00001SFTPClungMESH:D011625Pterygiumeye
HM00001SFTPClungMESH:D013610Tachycardia
HM00001SFTPClungMESH:D019851Thrombophiliabone marrow
HM00001SFTPClungMESH:D014802Vitamin A Deficiency
HM00001SFTPClungMESH:D003092Colitis
HM00001SFTPClungMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00001SFTPClungMESH:D012878Skin Neoplasms
HM00001SFTPClungMESH:D014376Tuberculosis
HM00001SFTPClungMESH:D005124Eye Abnormalities
HM00001SFTPClungMESH:D005832Genital Diseases, Maletestis
HM00001SFTPClungMESH:D005832Genital Diseases, Maleprostate
HM00001SFTPClungMESH:D005832Genital Diseases, Maleblood vessel
HM00001SFTPClungMESH:D014604Uveal Neoplasmseye
HM00001SFTPClungMESH:D000014Abnormalities, Drug-Induced
HM00001SFTPClungMESH:D019559Capillary Leak Syndromeskin
HM00001SFTPClungMESH:D003384Coxsackievirus Infections
HM00001SFTPClungMESH:D015352Dry Eye Syndromeseye
HM00001SFTPClungMESH:D006317Hearing Loss, Noise-Induced
HM00001SFTPClungMESH:D007249Inflammation
HM00001SFTPClungMESH:D000740Anemiabone marrow
HM00001SFTPClungMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM00001SFTPClungMESH:D007021Hypospadias
HM00001SFTPClungMESH:D054198Precursor Cell Lymphoblastic Leukemia-Lymphoma
HM00001SFTPClungMESH:D012208Rhabdomyosarcomarectum
HM00001SFTPClungMESH:D012208Rhabdomyosarcomaprostate
HM00001SFTPClungMESH:D012208Rhabdomyosarcomamuscle
HM00001SFTPClungMESH:D002277Carcinoma
HM00001SFTPClungMESH:D007008Hypokalemia
HM00001SFTPClungMESH:D001169Arthritis, Experimental
HM00001SFTPClungMESH:D008114Liver Neoplasms, Experimental
HM00001SFTPClungMESH:D014605Uveitiseye
HM00001SFTPClungMESH:D004487Edema
HM00001SFTPClungMESH:D007248Infertility, Male
HM00001SFTPClungMESH:D010382Peliosis Hepatisliver
HM00001SFTPClungMESH:D015619Respiratory System Abnormalities
HM00001SFTPClungMESH:D013276Stomach Ulcer
HM00001SFTPClungMESH:D007984Leydig Cell Tumor
HM00001SFTPClungMESH:D020326Migraine without Aurabrain
HM00001SFTPClungMESH:D020246Venous Thrombosis
HM00001SFTPClungMESH:D011472Prostatitisprostate
HM00001SFTPClungMESH:D013088Spermatocele
HM00001SFTPClungMESH:D006940Hyperemia
HM00001SFTPClungMESH:D013274Stomach Neoplasms
HM00001SFTPClungMESH:D001008Anxiety Disorders
HM00001SFTPClungMESH:D001249Asthmalung
HM00001SFTPClungMESH:D017880Limb Deformities, Congenital
HM00001SFTPClungMESH:D008106Liver Cirrhosis, Experimental
HM00001SFTPClungMESH:D000015Abnormalities, Multiple
HM00001SFTPClungMESH:D018281Cholangiocarcinomaliver
HM00001SFTPClungMESH:D003371Cough
HM00001SFTPClungMESH:D056486Drug-Induced Liver Injury
HM00001SFTPClungMESH:D008107Liver Diseasesskin
HM00001SFTPClungMESH:D008107Liver Diseasesmuscle
HM00001SFTPClungMESH:D008107Liver Diseaseslung
HM00001SFTPClungMESH:D008107Liver Diseasesliver
HM00001SFTPClungMESH:D016584Panic Disorder
HM00001SFTPClungMESH:D011297Prenatal Exposure Delayed Effects
HM00001SFTPClungMESH:D013927Thrombosis
HM00001SFTPClungMESH:D004485Eczema
HM00001SFTPClungMESH:D007938Leukemiaspleen
HM00001SFTPClungMESH:D007938Leukemiabone marrow
HM00001SFTPClungOMIM:265120SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1
HM00001SFTPClungMESH:D001321Autistic Disorder
HM00001SFTPClungMESH:D001836Body Weight Changes
HM00001SFTPClungMESH:D001997Bronchopulmonary Dysplasialung
HM00001SFTPClungMESH:D019586Intracranial Hypertensionbrain
HM00001SFTPClungMESH:D019586Intracranial Hypertensionblood vessel
HM00001SFTPClungMESH:D003110Colonic Neoplasmscolon
HM00001SFTPClungMESH:D006985Hyperventilation
HM00001SFTPClungMESH:D017119Porphyria Cutanea Tardaskin
HM00001SFTPClungMESH:D006528Carcinoma, Hepatocellularliver
HM00001SFTPClungMESH:D005234Fatty Liver
HM00001SFTPClungMESH:D008545Melanomaeye
HM00001SFTPClungMESH:D008545Melanomacervix
HM00001SFTPClungMESH:D008545Melanomabone
HM00001SFTPClungMESH:D002583Uterine Cervical Neoplasmscervix
HM00001SFTPClungMESH:D007569Jaw Abnormalities
HM00001SFTPClungMESH:D008527Medulloblastomaembryo
HM00001SFTPClungMESH:D008113Liver Neoplasms
HM00001SFTPClungMESH:D008113Liver Neoplasms
HM00001SFTPClungMESH:D012127Respiratory Distress Syndrome, Newbornlung
HM00001SFTPClungMESH:D015140Dementia, Vascular
HM00001SFTPClungMESH:D003967Diarrhea
HM00001SFTPClungMESH:D009436Neural Tube Defects
HM00001SFTPClungMESH:D002822Choriocarcinomabrain
HM00001SFTPClungMESH:D012772Shock, Septic
HM00001SFTPClungMESH:D000230Adenocarcinoma
HM00001SFTPClungMESH:D000230Adenocarcinomauterus
HM00001SFTPClungMESH:D000230Adenocarcinoma
HM00001SFTPClungMESH:D000230Adenocarcinoma
HM00001SFTPClungMESH:D000230Adenocarcinomauterus
HM00001SFTPClungMESH:D000230Adenocarcinomathyroid
HM00001SFTPClungMESH:D000230Adenocarcinomaskin
HM00001SFTPClungMESH:D000230Adenocarcinomaparathyroid gland
HM00001SFTPClungMESH:D000230Adenocarcinomaliver
HM00001SFTPClungMESH:D000230Adenocarcinomakidney
HM00001SFTPClungMESH:D000230Adenocarcinomaeye
HM00001SFTPClungMESH:D000230Adenocarcinomaadrenal gland
HM00001SFTPClungMESH:D001172Arthritis, Rheumatoidbone
HM00001SFTPClungMESH:D001848Bone Diseases, Developmental
HM00001SFTPClungMESH:D006330Heart Defects, Congenital
HM00001SFTPClungMESH:D008591Meningomyelocele
HM00001SFTPClungMESH:D017681Hypereosinophilic Syndrome
HM00001SFTPClungMESH:D008103Liver Cirrhosisliver
HM00001SFTPClungMESH:D010051Ovarian Neoplasmsuterus
HM00001SFTPClungMESH:D010051Ovarian Neoplasms
HM00001SFTPClungMESH:D020301Vasospasm, Intracranialblood vessel
HM00001SFTPClungMESH:D007247Infertility, Female
HM00001SFTPClungMESH:D009421Nervous System Malformations
HM00001SFTPClungMESH:D014594Uterine Neoplasmscervix
HM00001SFTPClungMESH:D014594Uterine Neoplasms