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 .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.374 Citrullinemia .
C12 Male Urogenital Diseases .
C12.706 Urogenital Abnormalities .
C12.706.316 Disorders of Sex Development .
C12.706.316.096 46, XY Disorders of Sex Development .
C12.706.316.096.500 Androgen-Insensitivity Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.875 Urogenital Abnormalities .
C13.351.875.253 Disorders of Sex Development .
C13.351.875.253.096 46, XY Disorders of Sex Development .
C13.351.875.253.096.500 Androgen-Insensitivity Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.939 Urogenital Abnormalities .
C16.131.939.316 Disorders of Sex Development .
C16.131.939.316.096 46, XY Disorders of Sex Development .
C16.131.939.316.096.500 Androgen-Insensitivity Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.061 Androgen-Insensitivity Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.940 Urea Cycle Disorders, Inborn .
C16.320.565.100.940.374 Citrullinemia .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.374 Citrullinemia .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.374 Citrullinemia .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.940 Urea Cycle Disorders, Inborn .
C18.452.648.100.940.374 Citrullinemia .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.374 Citrullinemia .
C18.654 Nutrition Disorders .
C18.654.521 Malnutrition .
C18.654.521.500 Deficiency Diseases .
C19 Endocrine System Diseases .
C19.391 Gonadal Disorders .
C19.391.119 Disorders of Sex Development .
C19.391.119.096 46, XY Disorders of Sex Development .
C19.391.119.096.500 Androgen-Insensitivity Syndrome .
SP6 Nutrition, Public Health .
SP6.016 Nutrition Disorders .
SP6.016.052 Deficiency Diseases .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Androgen-Insensitivity Syndrome .
AR Deficiency .
Androgen Insensitivity Syndrome .
Androgen Insensitivity, Partial .
Androgen Receptor Deficiency .
Androgen Resistance Syndrome .
Androgen-Insensitivity Syndrome, Complete .
Androgen-Insensitivity Syndrome, Partial .
DHTR Deficiency .
Dihydrotestosterone Receptor Deficiency .
Male Pseudohermaphroditism Due to Androgen Insensitivity .
Reifenstein Syndrome .
Reifenstein's Syndrome .
Testicular Feminization Syndrome .
AR Deficiencies .
Androgen Insensitivities, Partial .
Androgen Insensitivity Syndrome, Complete .
Androgen Insensitivity Syndrome, Partial .
Androgen Insensitivity Syndromes .
Androgen Receptor Deficiencies .
Androgen Resistance Syndromes .
Androgen-Insensitivity Syndromes .
Androgen-Insensitivity Syndromes, Complete .
Androgen-Insensitivity Syndromes, Partial .
Complete Androgen-Insensitivity Syndrome .
Complete Androgen-Insensitivity Syndromes .
DHTR Deficiencies .
Deficiencies, AR .
Deficiencies, Androgen Receptor .
Deficiencies, DHTR .
Deficiencies, Dihydrotestosterone Receptor .
Deficiency, AR .
Deficiency, Androgen Receptor .
Deficiency, DHTR .
Deficiency, Dihydrotestosterone Receptor .
Dihydrotestosterone Receptor Deficiencies .
Feminization Syndrome, Testicular .
Feminization Syndromes, Testicular .
Feminization, Testicular .
Feminizations, Testicular .
Insensitivities, Partial Androgen .
Insensitivity Syndrome, Androgen .
Insensitivity Syndromes, Androgen .
Insensitivity, Partial Androgen .
Partial Androgen Insensitivities .
Partial Androgen Insensitivity .
Partial Androgen-Insensitivity Syndrome .
Partial Androgen-Insensitivity Syndromes .
Receptor Deficiencies, Androgen .
Receptor Deficiencies, Dihydrotestosterone .
Receptor Deficiency, Androgen .
Receptor Deficiency, Dihydrotestosterone .
Reifensteins Syndrome .
Resistance Syndrome, Androgen .
Resistance Syndromes, Androgen .
Testicular Feminization Syndromes .
Testicular Feminizations .
Testicular Feminization .
1.00
401836
 
/deficiency .
0.70
 
Deficiency Diseases .
Deficiency Disease .
Disease, Deficiency .
Diseases, Deficiency .
0.61
1925906
 
Citrullinemia .
Argininosuccinic Acid Synthase Deficiency Disease .
Argininosuccinic Acid Synthetase Deficiency Disease .
Argininosuccinic Acid Synthetase Deficiency Disease, Partial .
Argininosuccinic Acid Synthetase Deficiency, Complete .
Citrullinemia, Classical .
Citrullinemia, Late-Onset .
Citrullinemia, Neonatal .
Citrullinemia, Type I .
Citrullinuria .
Complete Argininosuccinic Acid Synthetase Deficiency Disease .
Deficiency, Argininosuccinic Acid Synthetase, Complete .
Deficiency, Argininosuccinic Acid Synthetase, Partial .
Partial Argininosuccinic Acid Synthetase Deficiency Disease .
ASS Deficiencies .
Argininosuccinate Synthetase Deficiencies .
Citrullinemia, Late Onset .
Citrullinemias .
Citrullinemias, Classic .
Citrullinemias, Classical .
Citrullinemias, Late-Onset .
Citrullinemias, Neonatal .
Citrullinurias .
Classic Citrullinemia .
Classic Citrullinemias .
Classical Citrullinemia .
Classical Citrullinemias .
Deficiencies, ASS .
Deficiencies, Argininosuccinate Synthetase .
Deficiency, ASS .
Deficiency, Argininosuccinate Synthetase .
Late-Onset Citrullinemia .
Late-Onset Citrullinemias .
Neonatal Citrullinemia .
Neonatal Citrullinemias .
Type 1, Citrullinemia .
Argininosuccinate Synthase Deficiency Disease .
Argininosuccinate Synthetase Deficiency .
Argininosuccinic Acid Synthetase Deficiency .
ASS Deficiency .
Citrullinemia 1 .
Citrullinemia Type 1 .
Citrullinemia, Classic .
Deficiency Disease, Argininosuccinate Synthase .
Deficiency Disease, Argininosuccinic Acid Synthase .
0.58
6245