serw-MX  [xml]  
 


    
 Categorias DeCS

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.831 Skin Abnormalities .
C16.131.831.775 Rothmund-Thomson Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.300 Hyperbilirubinemia, Hereditary .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.765 Rothmund-Thomson Syndrome .
C16.614 Infant, Newborn, Diseases .
C16.614.760 Rothmund-Thomson Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.804 Skin Abnormalities .
C17.800.804.775 Rothmund-Thomson Syndrome .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.775 Rothmund-Thomson Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.284 DNA Repair-Deficiency Disorders .
C18.452.284.760 Rothmund-Thomson Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.300 Hyperbilirubinemia, Hereditary .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Rothmund-Thomson Syndrome .
Congenital Poikiloderma .
Poikiloderma Atrophicans and Cataract .
Poikiloderma Congenitale of Rothmund-Thomson .
Poikiloderma of Rothmund-Thomson .
Congenitale, Poikiloderma .
Congenitales, Poikiloderma .
Poikiloderma Congenitales .
Poikiloderma of Rothmund Thomson .
Rothmund Thomson Syndrome .
Rothmund-Thomson Poikiloderma .
Rothmund-Thomson Poikilodermas .
Syndrome, Rothmund-Thomson .
Poikiloderma Congenitale .
1.00
11453
 
Hyperbilirubinemia, Hereditary .
Hyperbilirubinemia, Rotor Type .
Hereditary Hyperbilirubinemia .
Hereditary Hyperbilirubinemias .
Hyperbilirubinemias, Hereditary .
Rotor Type Hyperbilirubinemia .
Syndrome, Rotor .
Rotor Syndrome .
0.56
10903