serw-MX  [xml]  
 


    
 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