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 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 .
C10.228.140.163.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.163.100.362.375 Canavan Disease .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.374 Citrullinemia .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.375 Canavan Disease .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.375 Canavan Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.300 Canavan Disease .
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 .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.150 Canavan Disease .
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 .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.375 Canavan Disease .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.374 Citrullinemia .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.100 Aspartylglucosaminuria .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.375 Canavan Disease .
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 .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.375 Canavan Disease .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.374 Citrullinemia .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.100 Aspartylglucosaminuria .
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 .
C19.787 Polyendocrinopathies, Autoimmune .
C20 Immune System Diseases .
C20.111 Autoimmune Diseases .
C20.111.750 Polyendocrinopathies, Autoimmune .
 
 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 .
0.73
 
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 .
0.68
6245
 
Canavan Disease .
ACY2 Deficiency .
ASP Deficiency .
ASPA Deficiency .
Aminoacylase 2 Deficiency .
Aspartoacylase Deficiency .
Canavan Disease, Familial Form .
Canavan Disease, Infantile .
Canavan Disease, Juvenile .
Canavan Disease, Neonatal .
Canavan Disease, Sporadic Form .
Canavan Disease, Type I .
Canavan Disease, Type II .
Canavan Disease, Type III .
Canavan-van Bogaert-Bertrand Disease .
Deficiency Disease, Aspartoacylase .
Familial Form of Canavan Disease .
Infantile Canavan Disease .
Juvenile Canavan Disease .
Leukodystrophy, Spongiform .
Neonatal Canavan Disease .
Spongy Degeneration Of Central Nervous System .
Spongy Degeneration of Infancy .
Spongy Degeneration of White Matter In Infancy .
Spongy Degeneration of the Brain .
Spongy Degeneration of the Central Nervous System .
Spongy Disease of Central Nervous System .
Spongy Disease of White Matter .
Sporadic Form of Canavan Disease .
Type I Canavan Disease .
Type II Canavan Disease .
Type III Canavan Disease .
Van Bogaert-Bertrand Syndrome .
Von Bogaert-Bertrand Disease .
Canavan van Bogaert Bertrand Disease .
Disease, Canavan .
Disease, Canavan-van Bogaert-Bertrand .
Disease, Von Bogaert-Bertrand .
Spongiform Leukodystrophy .
Syndrome, Van Bogaert-Bertrand .
Van Bogaert Bertrand Syndrome .
Von Bogaert Bertrand Disease .
Canavan-van Bogaert-Bertrand Disease .
Leukodystrophy, Spongiform .
Spongy Disease of White Matter .
0.66
1268
 
Aspartylglucosaminuria .
AGA Deficiency .
Aspartylglucosamidase Deficiency .
Aspartylglycosaminuria .
Glycoasparaginase .
AGA Deficiencies .
Aspartylglucosamidase Deficiencies .
Aspartylglucosaminurias .
Aspartylglycosaminurias .
Deficiencies, AGA .
Deficiencies, Aspartylglucosamidase .
Deficiency, AGA .
Deficiency, Aspartylglucosamidase .
Glycoasparaginases .
0.64
0114
 
Polyendocrinopathies, Autoimmune .
AIRE Deficiency .
APECED .
APS Type 1 .
Autoimmune Polyendocrine Syndrome, Type 2 .
Autoimmune Polyendocrine Syndrome, Type II .
Autoimmune Polyendocrinopathy Syndrome Type 1 .
Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy .
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy .
Autoimmune Polyglandular Syndrome Type I .
Autoimmune Polyglandular Syndrome Type II .
Autoimmune Polyglandular Syndrome Type III .
Autoimmune Polyglandular Syndrome, Type 1 .
Autoimmune Polyglandular Syndrome, Type 3 .
Autoimmune Polyglandular Syndrome, Type I .
Autoimmune Syndrome Type III, Polyglandular .
Diabetes Mellitus, Addison Disease, Myxedema .
Diabetes Mellitus, Addison's Disease, Myxedema .
Multiple Endocrine Deficiency Syndrome, Type 2 .
Polyendocrine Autoimmune Syndrome, Type II .
Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune .
Polyglandular Autoimmune Syndrome, Type 1 .
Polyglandular Autoimmune Syndrome, Type 2 .
Polyglandular Autoimmune Syndrome, Type 3 .
Polyglandular Autoimmune Syndrome, Type I .
Polyglandular Deficiency Syndrome, Type 2 .
Polyglandular Type III Autoimmune Syndrome .
Schmidt Syndrome .
AIRE Deficiencies .
Autoimmune Polyendocrinopathy .
Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy .
Deficiency, AIRE .
Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune .
Polyendocrinopathy, Autoimmune .
Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune .
Syndrome, Schmidt .
Syndrome, Schmidt's .
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy .
Autoimmune Syndrome Type I, Polyglandular .
Autoimmune Syndrome Type II, Polyglandular .
Polyglandular Type I Autoimmune Syndrome .
Polyglandular Type II Autoimmune Syndrome .
Schmidt's Syndrome .
0.63
281112