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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00003COL17A1pharynxMESH:D009396Wilms Tumorkidney
HM00003COL17A1pharynxMESH:D009396Wilms Tumorcervix
HM00003COL17A1pharynxMESH:D017880Limb Deformities, Congenital
HM00003COL17A1pharynxMESH:D003876Dermatitis, Atopicskin
HM00003COL17A1pharynxMESH:D010051Ovarian Neoplasmsuterus
HM00003COL17A1pharynxMESH:D010051Ovarian Neoplasms
HM00003COL17A1pharynxMESH:D001943Breast Neoplasmsbreast
HM00003COL17A1pharynxMESH:D002972Cleft Palate
HM00003COL17A1pharynxMESH:D001172Arthritis, Rheumatoidbone
HM00003COL17A1pharynxMESH:D001749Urinary Bladder Neoplasmsureter
HM00003COL17A1pharynxMESH:D001749Urinary Bladder Neoplasmsbladder
HM00003COL17A1pharynxMESH:D005909Glioblastomabone
HM00003COL17A1pharynxMESH:D005909Glioblastomabrain
HM00003COL17A1pharynxMESH:D005909Glioblastomabone
HM00003COL17A1pharynxMESH:D007569Jaw Abnormalities
HM00003COL17A1pharynxMESH:D017499Porokeratosisskin
HM00003COL17A1pharynxMESH:D004487Edema
HM00003COL17A1pharynxMESH:D008591Meningomyelocele
HM00003COL17A1pharynxMESH:D009421Nervous System Malformations
HM00003COL17A1pharynxMESH:D000152Acne Vulgaris
HM00003COL17A1pharynxMESH:D011297Prenatal Exposure Delayed Effects
HM00003COL17A1pharynxMESH:D009135Muscular Diseasesmuscle
HM00003COL17A1pharynxMESH:D009765Obesity
HM00003COL17A1pharynxMESH:D006529Hepatomegaly
HM00003COL17A1pharynxOMIM:226650EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE
HM00003COL17A1pharynxMESH:D005124Eye Abnormalities
HM00003COL17A1pharynxMESH:D008106Liver Cirrhosis, Experimental
HM00003COL17A1pharynxMESH:D009369Neoplasmsspleen
HM00003COL17A1pharynxMESH:D009369Neoplasmsbone marrow
HM00003COL17A1pharynxMESH:D001997Bronchopulmonary Dysplasialung
HM00003COL17A1pharynxMESH:D006943Hyperglycemia
HM00003COL17A1pharynxMESH:D005355Fibrosis
HM00003COL17A1pharynxMESH:D011596Psychomotor Disorders
HM00003COL17A1pharynxMESH:D010146Pain
HM00003COL17A1pharynxMESH:D014820Vitiligobone marrow
HM00003COL17A1pharynxMESH:D010190Pancreatic Neoplasmspancreas
HM00003COL17A1pharynxMESH:D012878Skin Neoplasms
HM00003COL17A1pharynxMESH:D014376Tuberculosis
HM00003COL17A1pharynxMESH:D002386Cataractpancreas
HM00003COL17A1pharynxMESH:D002386Cataracteye
HM00003COL17A1pharynxMESH:D019465Craniofacial Abnormalities
HM00003COL17A1pharynxMESH:D008545Melanomaeye
HM00003COL17A1pharynxMESH:D008545Melanomacervix
HM00003COL17A1pharynxMESH:D008545Melanomabone
HM00003COL17A1pharynxMESH:D013964Thyroid Neoplasmsthyroid
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmsthyroid
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmsskin
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmslarynx
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmsear
HM00003COL17A1pharynxMESH:D006258Head and Neck Neoplasmsbrain
HM00003COL17A1pharynxMESH:D006317Hearing Loss, Noise-Induced
HM00003COL17A1pharynxMESH:D006333Heart Failureheart
HM00003COL17A1pharynxMESH:D008175Lung Neoplasmslung
HM00003COL17A1pharynxMESH:D055371Acute Lung Injury
HM00003COL17A1pharynxMESH:D002294Carcinoma, Squamous Celllung
HM00003COL17A1pharynxMESH:D002294Carcinoma, Squamous Cellliver
HM00003COL17A1pharynxMESH:D002294Carcinoma, Squamous Celllarynx
HM00003COL17A1pharynxMESH:D002294Carcinoma, Squamous Cellkidney
HM00003COL17A1pharynxMESH:D002294Carcinoma, Squamous Celleye
HM00003COL17A1pharynxMESH:D017681Hypereosinophilic Syndrome
HM00003COL17A1pharynxMESH:D007410Intestinal Diseasessmall intestine
HM00003COL17A1pharynxMESH:D007410Intestinal Diseasesrectum
HM00003COL17A1pharynxMESH:D007410Intestinal Diseasescolon
HM00003COL17A1pharynxMESH:D007410Intestinal Diseasesblood vessel
HM00003COL17A1pharynxMESH:D008113Liver Neoplasms
HM00003COL17A1pharynxMESH:D008113Liver Neoplasms
HM00003COL17A1pharynxMESH:D009190Myelodysplastic Syndromes
HM00003COL17A1pharynxMESH:D011625Pterygiumeye
HM00003COL17A1pharynxMESH:D008527Medulloblastomaembryo
HM00003COL17A1pharynxMESH:D007938Leukemiaspleen
HM00003COL17A1pharynxMESH:D007938Leukemiabone marrow
HM00003COL17A1pharynxMESH:D006330Heart Defects, Congenital
HM00003COL17A1pharynxMESH:D009203Myocardial Infarctionheart
HM00003COL17A1pharynxMESH:D002583Uterine Cervical Neoplasmscervix
HM00003COL17A1pharynxMESH:D005234Fatty Liver
HM00003COL17A1pharynxMESH:D007951Leukemia, Myeloidbone marrow
HM00003COL17A1pharynxMESH:D009447Neuroblastomaeye
HM00003COL17A1pharynxMESH:D009447Neuroblastomabrain
HM00003COL17A1pharynxMESH:D000505Alopeciaskin
HM00003COL17A1pharynxMESH:D001471Barrett Esophagusesophagus
HM00003COL17A1pharynxMESH:D002822Choriocarcinomabrain
HM00003COL17A1pharynxMESH:D017486Acneiform Eruptions
HM00003COL17A1pharynxMESH:D018248Adenoma, Liver Cell
HM00003COL17A1pharynxMESH:D003092Colitis
HM00003COL17A1pharynxMESH:D015427Reperfusion Injury
HM00003COL17A1pharynxMESH:D014604Uveal Neoplasmseye
HM00003COL17A1pharynxMESH:D015473Leukemia, Promyelocytic, Acute
HM00003COL17A1pharynxMESH:D000014Abnormalities, Drug-Induced
HM00003COL17A1pharynxMESH:D001249Asthmalung
HM00003COL17A1pharynxMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM00003COL17A1pharynxMESH:D011507Proteinuriakidney
HM00003COL17A1pharynxMESH:D018290Cervical Intraepithelial Neoplasia
HM00003COL17A1pharynxMESH:D015428Myocardial Reperfusion Injury
HM00003COL17A1pharynxMESH:D009436Neural Tube Defects
HM00003COL17A1pharynxMESH:D016889Endometrial Neoplasmsuterus
HM00003COL17A1pharynxMESH:D014062Tongue Neoplasms
HM00003COL17A1pharynxMESH:D007333Insulin Resistance
HM00003COL17A1pharynxMESH:D006528Carcinoma, Hepatocellularliver
HM00003COL17A1pharynxMESH:D012208Rhabdomyosarcomarectum
HM00003COL17A1pharynxMESH:D012208Rhabdomyosarcomaprostate
HM00003COL17A1pharynxMESH:D012208Rhabdomyosarcomamuscle
HM00003COL17A1pharynxMESH:D001169Arthritis, Experimental
HM00003COL17A1pharynxMESH:D017492Keratosis, Seborrheicskin
HM00003COL17A1pharynxMESH:D008114Liver Neoplasms, Experimental
HM00003COL17A1pharynxMESH:D000015Abnormalities, Multiple
HM00003COL17A1pharynxMESH:D000236Adenomapancreas
HM00003COL17A1pharynxMESH:D000236Adenomaliver
HM00003COL17A1pharynxMESH:D000236Adenomakidney
HM00003COL17A1pharynxMESH:D000236Adenoma
HM00003COL17A1pharynxMESH:D000236Adenoma
HM00003COL17A1pharynxMESH:D000236Adenoma
HM00003COL17A1pharynxMESH:D000236Adenoma
HM00003COL17A1pharynxMESH:D002779Cholestasisliver
HM00003COL17A1pharynxMESH:D006930Hyperalgesia
HM00003COL17A1pharynxMESH:D013274Stomach Neoplasms
HM00003COL17A1pharynxMESH:D001778Blood Coagulation Disordersbone marrow
HM00003COL17A1pharynxMESH:D018236Carcinoma, Embryonal