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 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.550 Joint Diseases .
C05.550.150 Arthrogryposis .
C05.651 Muscular Diseases .
C05.651.102 Arthrogryposis .
C05.660 Musculoskeletal Abnormalities .
C05.660.077 Arthrogryposis .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.103 22q11 Deletion Syndrome .
C05.660.207.103.500 DiGeorge Syndrome .
C05.660.449 Hip Dislocation, Congenital .
C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.021 22q11 Deletion Syndrome .
C14.240.400.021.500 DiGeorge Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.044 22q11 Deletion Syndrome .
C14.280.400.044.500 DiGeorge 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 .
C15.378.190 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 .
C15.604 Lymphatic Diseases .
C15.604.451 Lymphatic Abnormalities .
C15.604.451.249 22q11 Deletion Syndrome .
C15.604.451.249.500 DiGeorge Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.019 22q11 Deletion Syndrome .
C16.131.077.019.500 DiGeorge Syndrome .
C16.131.077.350 Ectodermal Dysplasia .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.021 22q11 Deletion Syndrome .
C16.131.240.400.021.500 DiGeorge Syndrome .
C16.131.260 Chromosome Disorders .
C16.131.260.019 22q11 Deletion Syndrome .
C16.131.260.019.500 DiGeorge Syndrome .
C16.131.482 Lymphatic Abnormalities .
C16.131.482.249 22q11 Deletion Syndrome .
C16.131.482.249.500 DiGeorge Syndrome .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.077 Arthrogryposis .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.103 22q11 Deletion Syndrome .
C16.131.621.207.103.500 DiGeorge Syndrome .
C16.131.621.449 Hip Dislocation, Congenital .
C16.131.831 Skin Abnormalities .
C16.131.831.350 Ectodermal Dysplasia .
C16.320 Genetic Diseases, Inborn .
C16.320.077 Anemia, Hypoplastic, Congenital .
C16.320.077.090 Anemia, Diamond-Blackfan .
C16.320.180 Chromosome Disorders .
C16.320.180.019 22q11 Deletion Syndrome .
C16.320.180.019.500 DiGeorge Syndrome .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.250 Ectodermal Dysplasia .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.804 Skin Abnormalities .
C17.800.804.350 Ectodermal Dysplasia .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.250 Ectodermal Dysplasia .
C19 Endocrine System Diseases .
C19.642 Parathyroid Diseases .
C19.642.482 Hypoparathyroidism .
C19.642.482.500 22q11 Deletion Syndrome .
C19.642.482.500.500 DiGeorge Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Ectodermal Dysplasia .
Anhydrotic Ectodermal Dysplasia .
Aplasia Cutis Congenita, Nonsyndromic .
Autosomal Dominant Hidrotic Ectodermal Dysplasia .
Clouston Hidrotic Ectodermal Dysplasia .
Clouston Syndrome .
Clouston's Hidrotic Ectodermal Dysplasia .
Congenital Ectodermal Defect .
Defect, Congenital Ectodermal .
Ectodermal Dysplasia 2, Hidrotic .
Ectodermal Dysplasia Anhidrotic .
Ectodermal Dysplasia, Anhydrotic .
Ectodermal Dysplasia, Hidrotic .
Ectodermal Dysplasia, Hidrotic, Autosomal Dominant .
Hidrotic Ectodermal Dysplasia, Autosomal Dominant .
Hydrotic Ectodermal Dysplasia .
Anhidrotic Ectodermal Dysplasias .
Anhidrotic, Ectodermal Dysplasia .
Anhidrotics, Ectodermal Dysplasia .
Anhydrotic Ectodermal Dysplasias .
Cloustons Syndrome .
Congenital Ectodermal Defects .
Defects, Congenital Ectodermal .
Dysplasia Anhidrotic, Ectodermal .
Dysplasia Anhidrotics, Ectodermal .
Dysplasia, Anhidrotic Ectodermal .
Dysplasia, Anhydrotic Ectodermal .
Dysplasia, Ectodermal .
Dysplasia, Hidrotic Ectodermal .
Dysplasia, Hydrotic Ectodermal .
Dysplasias, Anhidrotic Ectodermal .
Dysplasias, Anhydrotic Ectodermal .
Dysplasias, Ectodermal .
Dysplasias, Hidrotic Ectodermal .
Dysplasias, Hydrotic Ectodermal .
Ectodermal Defects, Congenital .
Ectodermal Dysplasia, Anhidrotic .
Ectodermal Dysplasia, Hydrotic .
Ectodermal Dysplasias .
Ectodermal Dysplasias, Anhidrotic .
Ectodermal Dysplasias, Anhydrotic .
Ectodermal Dysplasias, Hydrotic .
Hidrotic Ectodermal Dysplasias .
Hydrotic Ectodermal Dysplasias .
Syndrome, Clouston .
Syndrome, Clouston's .
Ectodermal Defect, Congenital .
Anhidrotic Ectodermal Dysplasia .
Clouston's Syndrome .
Hidrotic Ectodermal Dysplasia .
Aplasia Cutis Congenita .
1.00
1782935
 
Hip Dislocation, Congenital .
Congenital Dysplasia Of The Hip .
Congenital Hip Dislocation .
Congenital Hip Displacement .
Congenital Hip Dysplasia .
Dislocation Of Hip, Congenital .
Dislocation, Congenital Hip .
Displacement, Congenital Hip .
Dysplasia, Congenital Hip .
Hip Displacement, Congenital .
Hip Dysplasia, Congenital, Nonsyndromic .
Hip, Dislocation Of, Congenital .
Congenital Hip Dislocations .
Congenital Hip Displacements .
Congenital Hip Dysplasias .
Dislocations, Congenital Hip .
Displacements, Congenital Hip .
Dysplasias, Congenital Hip .
Hip Dislocations, Congenital .
Hip Displacements, Congenital .
Hip Dysplasias, Congenital .
Hip Dysplasia, Congenital .
0.63
2576725
 
/abnormalities .
/agenesis .
/anomalies .
/aplasia .
/atresia .
/birth defects .
/congenital defects .
/defects .
/deformities .
/hypoplasia .
/malformations .
0.49
 
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 .
0.48
2362
 
Arthrogryposis .
Arthrogryposis Multiplex Congenita .
Arthrogryposis Multiplex Congenita (AMC) .
Congenital Arthromyodysplasia .
Congenital Multiple Arthrogryposis .
Fibrous Ankylosis of Multiple Joints .
Guérin-Stern Syndrome .
Otto Syndrome .
Rocher-Sheldon Syndrome .
Rossi Syndrome .
Arthrogryposes .
Arthrogryposes, Congenital Multiple .
Arthrogryposis Multiplex Congenitas .
Arthrogryposis Multiplex Congenitas (AMC) .
Arthrogryposis, Congenital Multiple .
Arthromyodysplasias, Congenital .
Congenita, Arthrogryposis Multiplex .
Congenita, Arthrogryposis Multiplex (AMC) .
Congenital Arthromyodysplasias .
Congenital Multiple Arthrogryposes .
Congenitas, Arthrogryposis Multiplex .
Congenitas, Arthrogryposis Multiplex (AMC) .
Guerin Stern Syndrome .
Guérin Stern Syndrome .
Multiple Arthrogryposes, Congenital .
Multiple Arthrogryposis, Congenital .
Multiplex Congenita, Arthrogryposis .
Multiplex Congenita, Arthrogryposis (AMC) .
Multiplex Congenitas, Arthrogryposis .
Multiplex Congenitas, Arthrogryposis (AMC) .
Rocher Sheldon Syndrome .
Syndrome, Guerin-Stern .
Syndrome, Guérin-Stern .
Syndrome, Otto .
Syndrome, Rocher-Sheldon .
Syndrome, Rossi .
Amyoplasia Congenita .
Arthromyodysplasia, Congenital .
Myodystrophia Fetalis Deformans .
Guerin-Stern Syndrome .
0.45
701592
 
/congenital .
/connatal .
/innate .
0.44
 
DiGeorge Syndrome .
22q11.2 Deletion Syndrome .
22q11.2DS .
Autosomal Dominant Opitz G-Bbb Syndrome .
Catch22 .
Conotruncal Anomaly Face Syndrome .
Conotruncal Anomaly Face Syndrome (CTAF) .
Deletion 22q11.2 Syndrome .
DiGeorge Anomaly .
DiGeorge Sequence .
Familial Third and Fourth Pharyngeal Pouch Syndrome .
Hypoplasia of Thymus and Parathyroids .
Pharyngeal Pouch Syndrome .
Sedlackova Syndrome .
Shprintzen Syndrome .
Shprintzen VCF Syndrome .
Third and Fourth Pharyngeal Pouch Syndrome .
Thymic Aplasia Syndrome .
VCF Syndrome .
Velo-Cardio-Facial Syndrome .
Autosomal Dominant Opitz G Bbb Syndrome .
Deletion Syndrome, 22q11.2 .
Syndrome, DiGeorge .
Syndrome, Sedlackova .
Syndrome, Shprintzen .
Syndrome, VCF .
Syndrome, Velo-Cardio-Facial .
Syndrome, Velocardiofacial .
Velo Cardio Facial Syndrome .
Velocardiofacial Syndrome .
0.44
581822