If you have problems viewing PDF files, download the latest version of Adobe Reader, For language access assistance, contact the NCATS Public Information Officer, Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311, expand submenu for Find Diseases By Category, expand submenu for Patients, Families and Friends, expand submenu for Healthcare Professionals. Ulcerative Colitis — see Inflammatory Bowel Disease. The RxList disease and condition listing contains explanations of many medical conditions and tests. Vaginal diseases can cause uncomfortable symptoms like itching, burning, and pain. Read more about which diseases are included on the GARD website. Por favor contáctenos. Index of comprehensive articles on medical diseases and conditions, o listing. Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. Disease articles are written by U.S. Board Certified Physicians. COVID-19 updates. To use the listing, browse the terms by selecting a letter. Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and products presented on the website. Centers for Disease Control and Prevention. CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website. You will be subject to the destination website's privacy policy when you follow the link. ©1996-2020 MedicineNet, Inc. All rights reserved. Read about vaginitis (inflammation) and other vaginal problems. Get the latest public health information from CDC: https://www.coronavirus.gov (link is external)
This list includes the main name for each condition, as well as alternate names. Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. Some conditions that are not, Ulna and fibula absence of with severe limb deficiency, Umbilical cord ulcer with intestinal atresia, Umbilical ulceration and intestinal atresia, UMOD-related autosomal dominant tubulointerstitial kidney disease, Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly, Undifferentiated connective tissue syndrome, Unicentric angiofollicular ganglionic hyperplasia, Unicentric angiofollicular lymph hyperplasia, Unilateral aplasia of the optic nerve with cryptophthalmus and contralateral microphthalmus, Unilateral defect of pectoralis muscle and syndactyly of the hand, Unilateral loss of facial flushing and sweating with contralateral anhidrosis, Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance, Unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies, Unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia, Unusual facial appearance, microcephaly, growth and mental retardation and syndactyly, Unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects, Unusual facies, cleft palate, mental retardation, and limb abnormalities, Unusual facies, cleft palate, short stature, and mental retardation, Unusual facies, digital abnormalities, and ichthyosis, Unusual facies, hooked clavicles, 13 pairs of ribs, widened metaphyses, square shaped vertebral bodies and communicating hydrocephalus, Upper limb malformations and congenital cardiac anomalies, Urea cycle disorder, arginino succinase type, Uridine diphosphate galactose-4-epimerase deficiency, Uridine monophosphate synthase deficiency, Uridine monophosphate synthetase deficiency, Uroporphyrinogen III synthase, deficiency of, Uveal coloboma-cleft lip/palate-mental retardation syndrome (formerly), Office of Rare Disease Research Facebook Page, Office of Rare Disease Research on Twitter, U.S. Department of Health & Human Services, Caring for Your Patient with a Rare Disease, Preguntas Más Frecuentes Sobre Enfermedades Raras, Como Encontrar un Especialista en su Enfermedad, Consejos Para una Condición no Diagnosticada, Consejos Para Obtener Ayuda Financiera Para Una Enfermedad, Preguntas Más Frecuentes Sobre los Trastornos Cromosómicos, Undifferentiated connective tissue disease, Febrile Ulceronecrotic Mucha-Habermann disease, Ulna hypoplasia-intellectual disability syndrome, Ulnar hypoplasia lobster claw deformity of feet, Umbilical cord ulceration and intestinal atresia, Autosomal dominant tubulointerstitial kidney disease due to UMOD mutations, Chromosome 1, uniparental disomy 1q12 q21, Cyprus facial neuromusculoskeletal syndrome, Ichthyosis tapered fingers midline groove up, Congenital thrombotic thrombocytopenic purpura, Prader-Willi habitus, osteopenia, and camptodactyly, Persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly, Uveal coloboma-cleft lip and palate-intellectual disability. Unicentric Castleman disease Unilateral absence of a pulmonary artery Unilateral agenesis of diaphragm - See Congenital diaphragmatic hernia Unilateral aplasia of the optic nerve with cryptophthalmus and contralateral microphthalmus - See Oculo-cerebral dysplasia No hemos publicado información en español sobre enfermedades que comiencen con esta letra. See additional information. Some conditions that are not considered rare are on this list and are labeled accordingly.
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