serw-MX  [xml]  
 
    
 Categorias DeCS

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.540 Menkes Kinky Hair Syndrome .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.687 Menkes Kinky Hair Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.071 Anemia .
C15.378.071.085 Anemia, Aplastic .
C15.378.071.085.080 Anemia, Hypoplastic, Congenital .
C15.378.071.085.080.090 Anemia, Diamond-Blackfan .
C15.378.071.750 Red-Cell Aplasia, Pure .
C15.378.071.750.500 Anemia, Diamond-Blackfan .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.056 Afibrinogenemia .
C15.378.100.141 Coagulation Protein Disorders .
C15.378.100.141.072 Afibrinogenemia .
C15.378.190 Bone Marrow Diseases .
C15.378.190.196 Anemia, Aplastic .
C15.378.190.196.080 Anemia, Hypoplastic, Congenital .
C15.378.190.196.080.090 Anemia, Diamond-Blackfan .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.067 Afibrinogenemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.077 Anemia, Hypoplastic, Congenital .
C16.320.077.090 Anemia, Diamond-Blackfan .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.056 Afibrinogenemia .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.687 Menkes Kinky Hair Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.687 Menkes Kinky Hair Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.540 Menkes Kinky Hair Syndrome .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.590 Menkes Kinky Hair Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.329 Hair Diseases .
C17.800.329.968 Menkes Kinky Hair Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.540 Menkes Kinky Hair Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.540 Menkes Kinky Hair Syndrome .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.590 Menkes Kinky Hair Syndrome .
 
 Termos
 Sinônimos e Históricos		Documentos
LILACS e MDL		 
Menkes Kinky Hair Syndrome .
Congenital Hypocupremia .
Copper Transport Disease .
Kinky Hair Disease .
Menkea Syndrome .
Menkes Disease .
Menkes' Disease .
Steely Hair Disease .
X-Linked Copper Deficiency .
Congenital Hypocupremias .
Copper Deficiencies, X-Linked .
Copper Deficiency, X-Linked .
Copper Transport Diseases .
Deficiencies, X-Linked Copper .
Deficiency, X-Linked Copper .
Disease, Copper Transport .
Disease, Steely Hair .
Diseases, Copper Transport .
Diseases, Kinky Hair .
Diseases, Menkes' .
Diseases, Steely Hair .
Hair Diseases, Kinky .
Hair Diseases, Steely .
Hypocupremias, Congenital .
Kinky Hair Diseases .
Menkea Syndromes .
Menkes' Diseases .
Steely Hair Diseases .
Steely Hair Syndromes .
Syndrome, Menkea .
Syndrome, Steely Hair .
Syndromes, Menkea .
Syndromes, Steely Hair .
Transport Disease, Copper .
Transport Diseases, Copper .
X Linked Copper Deficiency .
X-Linked Copper Deficiencies .
Menkes Syndrome .
Steely Hair Syndrome .
Kinky Hair Syndrome .
Hypocupremia, Congenital .
1.00
 
Afibrinogenemia .
Afibrinogenemia, Congenital .
Congenital Afibrinogenaemia .
Congenital Afibrinogenemia .
Deficiency, Fibrinogen .
Familial Afibrinogenemia .
Hypofibrinogenemia, Congenital .
Afibrinogenaemia, Congenital .
Afibrinogenaemias, Congenital .
Afibrinogenemia, Familial .
Afibrinogenemias .
Afibrinogenemias, Congenital .
Afibrinogenemias, Familial .
Congenital Afibrinogenaemias .
Congenital Afibrinogenemias .
Congenital Hypofibrinogenemia .
Congenital Hypofibrinogenemias .
Familial Afibrinogenemias .
Fibrinogen Deficiencies .
Hypofibrinogenemias, Congenital .
Fibrinogen Deficiency .
0.64
 
Anemia, Diamond-Blackfan .
Anemia, Congenital Hypoplastic, Of Blackfan And Diamond .
Anemia, Diamond-Blackfan Type .
Blackfan Diamond Anemia .
Blackfan-Diamond Disease .
Blackfan-Diamond Syndrome .
Chronic Congenital Agenerative Anemia .
Congenital Erythroid Hypoplastic Anemia .
Congenital Hypoplastic Anemia of Blackfan and Diamond .
Congenital Pure Red Cell Anemia .
Congenital Pure Red Cell Aplasia .
Erythrogenesis Imperfecta .
Hypoplastic Congenital Anemia .
Inherited Erythroblastopenia .
Pure Hereditary Red Cell Aplasia .
Red Cell Aplasia, Pure, Hereditary .
Anemia, Blackfan Diamond .
Anemia, Diamond Blackfan .
Anemia, Diamond Blackfan Type .
Anemia, Hypoplastic Congenital .
Anemias, Hypoplastic Congenital .
Blackfan Diamond Disease .
Blackfan Diamond Syndrome .
Congenital Anemia, Hypoplastic .
Congenital Anemias, Hypoplastic .
Diamond Anemia, Blackfan .
Diamond Blackfan Anemia .
Diamond-Blackfan Type Anemia .
Disease, Blackfan-Diamond .
Erythroblastopenia, Inherited .
Erythroblastopenias, Inherited .
Erythrogenesis Imperfectas .
Hypoplastic Congenital Anemias .
Imperfecta, Erythrogenesis .
Imperfectas, Erythrogenesis .
Inherited Erythroblastopenias .
Diamond-Blackfan Anemia .
0.63
 
Anemia, Hypoplastic, Congenital .
Anemia, Congenital Hypoplastic .
Anemias, Congenital Hypoplastic .
Congenital Hypoplastic Anemias .
Hypoplastic Anemias, Congenital .
Congenital Hypoplastic Anemia .
Hypoplastic Anemia, Congenital .
0.63