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Crigler-Najjar Syndrome, Type I CID10 - Classificação Internacional de Doenças DeCS Português DeCS Inglês DeCS Espanhol DeCS Espanha DeCS Português com escopo DeCS Inglês com escopo DeCS Espanhol com escopo DeCS Espanha com escopo LILACS - LILACS Regional
Categorias DeCS C05 Musculoskeletal Diseases . C05.116 Bone Diseases . C05.116.099 Bone Diseases, Developmental . C05.116.099.343 Dwarfism . C05.116.099.343.250 Cockayne Syndrome . C05.116.099.674 Marfan Syndrome . C09 Otorhinolaryngologic Diseases . C09.218 Ear Diseases . C09.218.458 Hearing Disorders . C09.218.458.341 Hearing Loss . C09.218.458.341.186 Deafness . C09.218.458.341.186.500 Deaf-Blind Disorders . C09.218.458.341.186.500.500 Usher Syndromes . C09.218.458.341.887 Hearing Loss, Sensorineural . C09.218.458.341.887.886 Usher Syndromes . C10 Nervous System Diseases . C10.574 Neurodegenerative Diseases . C10.574.500 Heredodegenerative Disorders, Nervous System . C10.574.500.362 Cockayne Syndrome . C10.597 Neurologic Manifestations . C10.597.751 Sensation Disorders . C10.597.751.418 Hearing Disorders . C10.597.751.418.341 Hearing Loss . C10.597.751.418.341.186 Deafness . C10.597.751.418.341.186.500 Deaf-Blind Disorders . C10.597.751.418.341.186.500.500 Usher Syndromes . C10.597.751.418.341.887 Hearing Loss, Sensorineural . C10.597.751.418.341.887.886 Usher Syndromes . C10.597.751.941 Vision Disorders . C10.597.751.941.162 Blindness . C10.597.751.941.162.625 Deaf-Blind Disorders . C10.597.751.941.162.625.500 Usher Syndromes . C11 Eye Diseases . C11.768 Retinal Diseases . C11.768.585 Retinal Degeneration . C11.768.585.658 Retinal Dystrophies . C11.768.585.658.500 Retinitis Pigmentosa . C11.768.585.658.500.813 Usher Syndromes . C11.966 Vision Disorders . C11.966.075 Blindness . C11.966.075.375 Deaf-Blind Disorders . C11.966.075.375.500 Usher Syndromes . C14 Cardiovascular Diseases . C14.240 Cardiovascular Abnormalities . C14.240.400 Heart Defects, Congenital . C14.240.400.725 Marfan Syndrome . C14.280 Heart Diseases . C14.280.400 Heart Defects, Congenital . C14.280.400.725 Marfan Syndrome . C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities . C16.131 Congenital Abnormalities . C16.131.077 Abnormalities, Multiple . C16.131.077.250 Cockayne Syndrome . C16.131.077.299 Deaf-Blind Disorders . C16.131.077.299.500 Usher Syndromes . C16.131.077.550 Marfan Syndrome . C16.131.240 Cardiovascular Abnormalities . C16.131.240.400 Heart Defects, Congenital . C16.131.240.400.720 Marfan Syndrome . C16.320 Genetic Diseases, Inborn . C16.320.240 Dwarfism . C16.320.240.562 Cockayne Syndrome . C16.320.290 Eye Diseases, Hereditary . C16.320.290.684 Retinitis Pigmentosa . C16.320.290.684.500 Usher Syndromes . C16.320.400 Heredodegenerative Disorders, Nervous System . C16.320.400.200 Cockayne Syndrome . C16.320.540 Marfan Syndrome . C16.320.565 Metabolism, Inborn Errors . C16.320.565.300 Hyperbilirubinemia, Hereditary . C16.320.565.300.281 Crigler-Najjar Syndrome . C17 Skin and Connective Tissue Diseases . C17.300 Connective Tissue Diseases . C17.300.500 Marfan Syndrome . C18 Nutritional and Metabolic Diseases . C18.452 Metabolic Diseases . C18.452.284 DNA Repair-Deficiency Disorders . C18.452.284.250 Cockayne Syndrome . C18.452.648 Metabolism, Inborn Errors . C18.452.648.300 Hyperbilirubinemia, Hereditary . C18.452.648.300.281 Crigler-Najjar Syndrome . C23 Pathological Conditions, Signs and Symptoms . C23.888 Signs and Symptoms . C23.888.592 Neurologic Manifestations . C23.888.592.763 Sensation Disorders . C23.888.592.763.393 Hearing Disorders . C23.888.592.763.393.341 Hearing Loss . C23.888.592.763.393.341.887 Hearing Loss, Sensorineural . C23.888.592.763.393.341.887.886 Usher Syndromes .		Termos  Sinônimos e Históricos Documentos LILACS e MDL   Crigler-Najjar Syndrome . Crigler Najjar Syndrome . Crigler Najjar Syndrome, Type 1 . Crigler-Najar Syndrome . Crigler-Najjar Syndrome, Type I . Familial Nonhemolytic Unconjugated Hyperbilirubinemia . Hereditary Unconjugated Hyperbilirubinemia . Crigler Najar Syndrome . Crigler Najjar Syndrome, Type I . 1.00   Marfan Syndrome . Marfan Syndrome, Type I . Marfan's Syndrome . Marfans Syndrome . Syndrome, Marfan . Syndrome, Marfan's . 0.51   Usher Syndromes . Deafness-Retinitis Pigmentosa Syndrome . Dystrophia Retinae Pigmentosa-Dysostosis Syndrome . Graefe-Usher Syndrome . Hallgren Syndrome . Retinitis Pigmentosa And Congenital Deafness . Retinitis Pigmentosa-Deafness Syndrome . Usher Syndrome . Usher Syndrome, Type 1 . Usher Syndrome, Type 1A . Usher Syndrome, Type 3 . Usher Syndrome, Type I . Usher Syndrome, Type I, French Variety . Usher Syndrome, Type II . Usher Syndrome, Type III . Usher Syndrome, Type IId . Usher's Syndrome . Deafness Retinitis Pigmentosa Syndrome . Deafness-Retinitis Pigmentosa Syndromes . Dystrophia Retinae Pigmentosa Dysostosis Syndrome . Graefe Usher Syndrome . Pigmentosa Syndromes, Deafness-Retinitis . Retinitis Pigmentosa Deafness Syndrome . Retinitis Pigmentosa-Deafness Syndromes . Syndrome, Deafness-Retinitis Pigmentosa . Syndrome, Graefe-Usher . Syndrome, Hallgren . Syndrome, Retinitis Pigmentosa-Deafness . Syndrome, Usher . Syndrome, Usher's . Syndromes, Deafness-Retinitis Pigmentosa . Syndromes, Retinitis Pigmentosa-Deafness . Syndromes, Usher . Ushers Syndrome . 0.50   Cockayne Syndrome . Cockayne Syndrome Type 3 . Cockayne Syndrome Type C . Cockayne Syndrome, Group A . Cockayne Syndrome, Group B . Cockayne Syndrome, Group C . Cockayne Syndrome, Type A . Cockayne Syndrome, Type B . Cockayne Syndrome, Type C . Cockayne Syndrome, Type I . Cockayne Syndrome, Type II . Cockayne Syndrome, Type III . Dwarfism-Retinal Atrophy-Deafness Syndrome . Group A Cockayne Syndrome . Group B Cockayne Syndrome . Group C Cockayne Syndrome . Progeroid Nanism . Type A Cockayne Syndrome . Type B Cockayne Syndrome . Type C Cockayne Syndrome . Type I Cockayne Syndrome . Type II Cockayne Syndrome . Type III Cockayne Syndrome . Progeria Like Syndrome . Progeria-Like Syndromes . Syndrome, Cockayne . Syndrome, Progeria-Like . Progeria-Like Syndrome . DWARFISM, CACHECTIC . 0.49