92
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Xylosyltransferase 1 |
DBQD2, PXYLT1, XT-I, XT1, XTI, XYLTI, xylT-I |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Pseudoxanthoma elasticum, Bone fragility with contractures, arterial rupture, and deafness, Graft versus host disease, Color vision deficiency, Corneal astigmatism, Dementia, Desbuquois dysplasia, Desbuquois syndrome, Diabetes mellitus type 1, Duchenne muscular dystrophy, Dyslexia, Erectile dysfunction, Larsen syndrome, Major depressive disorder, Obesity, Oligodendroglioma, Osteoporosis-pseudoglioma syndrome, Psoriasis, Sarcoidosis, Spondylosis, Substance abuse, Tourette syndrome, Diabetes mellitus type 2, Vascular dementia, Congenital disorder of glycosylation
Unreviewed: Acne, Age-related macular degeneration, Angioid streaks, Aortic Aneurysm, Arnold-Chiari malformation, Arthritis, Astrocytoma, Barber Say Syndrome, Bernard Soulier Syndrome, Blood coagulation disorder, Brooke-Spiegler Syndrome, Camptodactyly of fingers, Cartilage disease, Chondrosarcoma, Chronic disease, Clinodactyly, Congenital Disorder Of Glycosylation, Congenital Epicanthus, Congenital genu recurvatum, Congestive Heart Failure, Desbuquois Dysplasia, Desbuquois Syndrome, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetic Nephropathy, Diabetic neuropathy, Dilated cardiomyopathy, Drusen, Duchenne Muscular Dystrophy, Dwarfism, Dysmorphic Features, Epiphyseal dysplasia, Facial dysmorphism, Glaucoma, Growth disorder, Heart disease, Hypertension, Hypertrophy, Hypodontia, Hypotrichosis, Insulin-Like Growth Factor I Deficiency, Intervertebral Disc Degeneration, Isolated Somatotropin Deficiency, Kidney Disease, Leukemia, Liver cirrhosis, Macrocephaly, Mental retardation, Microcephaly, Mitral Valve Prolapse, Mitral Valve Stenosis, Mouth Abnormalities, Mucopolysaccharidosis, Myopia, Osteoarthritis, Osteochondrodysplasia, Platelet disorder, Proptosis, Radioulnar Synostosis, Renal Insufficiency, Restrictive cardiomyopathy, Scoliosis, Short clavicles, Skeletal Dysplasia, Somatotropin Deficiency, Spondyloepiphyseal dysplasia, Stroke, Synophrys, Systemic sclerosis, Ventricular septal defect
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93
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Xylosyltransferase 2 |
PXYLT2, SOS, XT-II, XT2, xylT-II |
Curated: Pseudoxanthoma elasticum, Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Larsen syndrome, Marshall syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome
Unreviewed: Age-related macular degeneration, Angioid streaks, Ataxia Telangiectasia, Atrial Septal Defect, Bladder carcinoma, Bladder Neoplasm, Cataract, Cerebral Infarction, Congenital heart defect, Congestive Heart Failure, Desbuquois Syndrome, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Drusen, Dysmorphic Features, Ewing sarcoma, Eye abnormalities, Fatty Liver, Graft-Vs-Host Disease, Hearing Loss, Hepatic veno-occlusive disease-immunodeficiency syndrome, Hepatocellular carcinoma, Hyperbilirubinemia, Hypertension, Kidney Disease, Leukemia, Lipodystrophy, Malignant Neoplasm, Mental Depression, Mental retardation, Microphthalmos, Mitral Valve Prolapse, Mitral Valve Stenosis, Mouth Abnormalities, Mucopolysaccharidosis, Multiple Congenital Anomalies, Myelomonocytic Leukemia, Myopia, Neck Webbing, Neoplasms, Noonan Syndrome, Nystagmus, Obesity, Osteopenia, Osteoporosis, Papilloma, Parkinson disease, Posteriorly Rotated Ear, Psoriatic Arthritis, Renal Insufficiency, Restrictive cardiomyopathy, Retinal Detachment, Scleroderma, Skin disease, Skin Lesion, Skin Neoplasms, Spondyloocular Syndrome, Stroke, Subarachnoid hemorrhage, Trichohepatoenteric Syndrome, Urinary bladder cancer, Ventricular septal defect, Xeroderma Pigmentosum
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