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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 .
C10.228.140.163.100.362.550 Leukodystrophy, Metachromatic .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.850 Sulfatidosis .
C10.228.140.163.100.435.825.850.500 Leukodystrophy, Metachromatic .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.124 Argininosuccinic Aciduria .
C10.228.140.163.100.937.374 Citrullinemia .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.550 Leukodystrophy, Metachromatic .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.550 Leukodystrophy, Metachromatic .
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 .
C16.320.565.100.940.124 Argininosuccinic Aciduria .
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 .
C16.320.565.189.362.550 Leukodystrophy, Metachromatic .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.850 Sulfatidosis .
C16.320.565.189.435.825.850.500 Leukodystrophy, Metachromatic .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.124 Argininosuccinic Aciduria .
C16.320.565.189.937.374 Citrullinemia .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.925 Sulfatidosis .
C16.320.565.398.641.803.925.500 Leukodystrophy, Metachromatic .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.100 Aspartylglucosaminuria .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.850 Sulfatidosis .
C16.320.565.595.554.825.850.500 Leukodystrophy, Metachromatic .
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 .
C18.452.132.100.362.550 Leukodystrophy, Metachromatic .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.850 Sulfatidosis .
C18.452.132.100.435.825.850.500 Leukodystrophy, Metachromatic .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.124 Argininosuccinic Aciduria .
C18.452.132.100.937.374 Citrullinemia .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.925 Sulfatidosis .
C18.452.584.687.803.925.500 Leukodystrophy, Metachromatic .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.940 Urea Cycle Disorders, Inborn .
C18.452.648.100.940.124 Argininosuccinic Aciduria .
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 .
C18.452.648.189.362.550 Leukodystrophy, Metachromatic .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.850 Sulfatidosis .
C18.452.648.189.435.825.850.500 Leukodystrophy, Metachromatic .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.124 Argininosuccinic Aciduria .
C18.452.648.189.937.374 Citrullinemia .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.925 Sulfatidosis .
C18.452.648.398.641.803.925.500 Leukodystrophy, Metachromatic .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.100 Aspartylglucosaminuria .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.850 Sulfatidosis .
C18.452.648.595.554.825.850.500 Leukodystrophy, Metachromatic .
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 .
 
 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
 
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 .
0.72
6245
 
Aspartylglucosaminuria .
AGA Deficiency .
Aspartylglucosamidase Deficiency .
Aspartylglycosaminuria .
Glycoasparaginase .
AGA Deficiencies .
Aspartylglucosamidase Deficiencies .
Aspartylglucosaminurias .
Aspartylglycosaminurias .
Deficiencies, AGA .
Deficiencies, Aspartylglucosamidase .
Deficiency, AGA .
Deficiency, Aspartylglucosamidase .
Glycoasparaginases .
0.68
0114
 
Argininosuccinic Aciduria .
ASA Deficiency .
ASL Deficiency .
Argininosuccinase Deficiency .
Argininosuccinate Acidemia .
Argininosuccinate Lyase Deficiency .
Argininosuccinic Acid Lyase Deficiency .
Argininosuccinic Acidemia .
Argininosuccinicaciduria .
Argininosuccinyl-Coa Lyase Deficiency .
Arginosuccinase Deficiency .
Asauria .
Inborn Error of Urea Synthesis, Arginino Succinic Type .
Urea Cycle Disorder, Arginino Succinase Type .
ASA Deficiencies .
ASL Deficiencies .
Acidemia, Argininosuccinate .
Acidemias, Argininosuccinate .
Aciduria, Argininosuccinic .
Acidurias, Argininosuccinic .
Arginino Succinase Deficiencies .
Argininosuccinate Acidemias .
Argininosuccinate Lyase Deficiencies .
Argininosuccinic Acidurias .
Argininosuccinicacidurias .
Deficiencies, ASA .
Deficiencies, ASL .
Deficiencies, Arginino Succinase .
Deficiencies, Argininosuccinate Lyase .
Deficiency, ASA .
Deficiency, ASL .
Deficiency, Arginino Succinase .
Deficiency, Argininosuccinate Lyase .
Arginino Succinase Deficiency .
0.67
0137
 
/deficiency .
0.66
 
Leukodystrophy, Metachromatic .
ARSA Deficiency .
Arylsulfatase A Deficiency .
Cerebral sclerosis, Diffuse, Metachromatic Form .
Cerebroside Sulfatase Deficiency .
Greenfield Disease .
Greenfield's Disease .
Leukodystrophy, Metachromatic, Adult .
Leukodystrophy, Metachromatic, Juvenile .
Metachromatic Leukodystrophy .
Metachromatic Leukodystrophy, Adult .
Metachromatic Leukodystrophy, Adult-Type .
Metachromatic Leukodystrophy, Infant .
Metachromatic Leukodystrophy, Infant-Type .
Metachromatic Leukodystrophy, Juvenile .
Metachromatic Leukodystrophy, Juvenile-Type .
Metachromatic Leukodystrophy, Late Infantile .
Metachromatic Leukoencephalopathy .
Sulfatide Lipidosis .
ARSA Deficiencies .
Adult Metachromatic Leukodystrophies .
Adult Metachromatic Leukodystrophy .
Adult-Type Metachromatic Leukodystrophies .
Adult-Type Metachromatic Leukodystrophy .
Arylsulfatase A Deficiencies .
Cerebroside Sulfatase Deficiencies .
Deficiencies, ARSA .
Deficiencies, Arylsulfatase A .
Deficiencies, Cerebroside Sulfatase .
Deficiency, ARSA .
Deficiency, Arylsulfatase A .
Deficiency, Cerebroside Sulfatase .
Infant Metachromatic Leukodystrophies .
Infant Metachromatic Leukodystrophy .
Infant-Type Metachromatic Leukodystrophies .
Infant-Type Metachromatic Leukodystrophy .
Juvenile Metachromatic Leukodystrophies .
Juvenile Metachromatic Leukodystrophy .
Juvenile-Type Metachromatic Leukodystrophies .
Juvenile-Type Metachromatic Leukodystrophy .
Leukodystrophies, Adult Metachromatic .
Leukodystrophies, Adult-Type Metachromatic .
Leukodystrophies, Juvenile Metachromatic .
Leukodystrophies, Juvenile-Type Metachromatic .
Leukodystrophies, Metachromatic .
Leukodystrophy, Adult Metachromatic .
Leukodystrophy, Adult-Type Metachromatic .
Leukodystrophy, Juvenile Metachromatic .
Leukodystrophy, Juvenile-Type Metachromatic .
Leukoencephalopathies, Metachromatic .
Leukoencephalopathy, Metachromatic .
Lipidosis, Sulfatide .
Metachromatic Leukodystrophies .
Metachromatic Leukodystrophies, Adult .
Metachromatic Leukodystrophies, Adult-Type .
Metachromatic Leukodystrophies, Infant .
Metachromatic Leukodystrophies, Infant-Type .
Metachromatic Leukodystrophies, Juvenile .
Metachromatic Leukodystrophies, Juvenile-Type .
Metachromatic Leukodystrophy, Adult Type .
Metachromatic Leukodystrophy, Infant Type .
Metachromatic Leukodystrophy, Juvenile Type .
Metachromatic Leukoencephalopathies .
Sulfatase Deficiencies, Cerebroside .
Sulfatase Deficiency, Cerebroside .
Arylsulfatase A Deficiency Disease .
Cerebroside Sulphatase Deficiency Disease .
0.66
161123