serw-MX  [xml]  
 


    
 DeCS Categories

C04 Neoplasms .
C04.588 Neoplasms by Site .
C04.588.322 Endocrine Gland Neoplasms .
C04.588.322.078 Adrenal Gland Neoplasms .
C04.588.322.078.265 Adrenal Cortex Neoplasms .
C04.588.322.078.265.500 Adrenocortical Adenoma .
C05 Musculoskeletal Diseases .
C05.550 Joint Diseases .
C05.550.114 Arthritis .
C05.550.114.122 Arthritis, Juvenile .
C05.651 Muscular Diseases .
C05.651.662 Myotonic Disorders .
C05.799 Rheumatic Diseases .
C05.799.056 Arthritis, Juvenile .
C10 Nervous System Diseases .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.606 Myotonic Disorders .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.364 Dent Disease .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.364 Dent Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.100 Dent Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.520 Glycogen Storage Disease Type III .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.271 Dent Disease .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.775 Rheumatic Diseases .
C17.300.775.049 Arthritis, Juvenile .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.520 Glycogen Storage Disease Type III .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.271 Dent Disease .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.098 Adrenal Cortex Diseases .
C19.053.098.265 Adrenal Cortex Neoplasms .
C19.053.098.265.500 Adrenocortical Adenoma .
C19.053.347 Adrenal Gland Neoplasms .
C19.053.347.500 Adrenal Cortex Neoplasms .
C19.053.347.500.500 Adrenocortical Adenoma .
C19.344 Endocrine Gland Neoplasms .
C19.344.078 Adrenal Gland Neoplasms .
C19.344.078.265 Adrenal Cortex Neoplasms .
C19.344.078.265.500 Adrenocortical Adenoma .
C20 Immune System Diseases .
C20.111 Autoimmune Diseases .
C20.111.198 Arthritis, Juvenile .
D02 Organic Chemicals .
D02.065 Amides .
D02.065.199 Anilides .
D02.065.199.420 Flutamide .
D02.092 Amines .
D02.092.146 Aniline Compounds .
D02.092.146.113 Anilides .
D02.092.146.113.420 Flutamide .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Myotonic Disorders .
Eulenburg Disease .
Eulenburg's Disease .
Paralysis Periodica Paramyotonia .
Paramyotonia Congenita Without Cold Paralysis .
Paramyotonia Congenita of von Eulenberg .
Von Eulenberg's Disease .
Disorder, Myotonic .
Disorders, Myotonic .
Myopathy, Myotonic .
Myotonic Disorder .
Myotonic Myopathies .
Myotonic Myopathy .
Von Eulenberg Disease .
Myopathies, Myotonic .
Myotonia Fluctuans .
Paramyotonia Congenita .
Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. .
1.00
2242
 
Dent Disease .
Dents Disease .
Disease, Dent .
Disease, Dent's .
Disease, Dents .
Dent's Disease .
X-linked recessive NEPHROLITHIASIS characterized by HYPERCALCIURIA; HYPOPHOSPHATEMIA; NEPHROCALCINOSIS; and PROTEINURIA. It is associated with mutations in the voltage-gated chloride channel, CLC-5 (Dent Disease I). Another group of mutations associated with this disease is in phosphatidylinositol 4,5-bisphosphate-5-phosphatase gene. .
0.50
252
 
Adrenocortical Adenoma .
Adenoma, Adrenocortical .
Conn Adenoma .
Conn Disease .
Adenoma, Conn .
Adenomas, Adrenal Cortical .
Adenomas, Adrenocortical .
Adenomas, Conn .
Adrenal Cortical Adenoma .
Adrenal Cortical Adenomas .
Adrenocortical Adenomas .
Conn Adenomas .
Conns Disease .
Disease, Conn .
Disease, Conn's .
Adenoma, Adrenal Cortical .
Conn's Disease .
A benign neoplasm of the ADRENAL CORTEX. It is characterized by a well-defined nodular lesion, usually less than 2.5 cm. Most adrenocortical adenomas are nonfunctional. The functional ones are yellow and contain LIPIDS. Depending on the cell type or cortical zone involved, they may produce ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. .
0.50
401009
 
Flutamide .
Apimid .
Apo-Flutamide .
Chimax .
Cytamid .
Drogenil .
Euflex .
Eulexin .
Eulexine .
Fluken .
Flulem .
Flumid .
Fluta 1A Pharma .
Fluta-GRY .
Fluta-cell .
Flutamin .
Flutandrona .
Flutaplex .
Flutexin .
Fugerel .
Grisetin .
Niftolide .
Novo-Flutamide .
Oncosal .
PMS-Flutamide .
Prostacur .
Prostica .
Prostogenat .
SCH-13521 .
Testotard .
Apo Flutamide .
ApoFlutamide .
Fluta GRY .
Fluta cell .
FlutaGRY .
Flutacell .
Novo Flutamide .
NovoFlutamide .
PMS Flutamide .
SCH 13521 .
SCH13521 .
Niftolid .
SCH-13521 .
An antiandrogen with about the same potency as cyproterone in rodent and canine species. .
0.50
442533
 
Glycogen Storage Disease Type III .
Amylo-1,6-Glucosidase Deficiency .
Cori Disease .
Deficiency, Debrancher .
Glycogen Debrancher Deficiency .
Glycogen Storage Disease III .
Glycogen Storage Disease Type 3 .
Amylo 1,6 Glucosidase Deficiency .
Amylo-1,6-Glucosidase Deficiencies .
Coris Disease .
Debrancher Deficiencies .
Debrancher Deficiencies, Glycogen .
Debrancher Deficiency, Glycogen .
Deficiencies, Amylo-1,6-Glucosidase .
Deficiencies, Debrancher .
Deficiencies, Glycogen Debrancher .
Deficiency, Amylo-1,6-Glucosidase .
Deficiency, Glycogen Debrancher .
Dextrinoses, Limit .
Dextrinosis, Limit .
Disease, Cori .
Disease, Cori's .
Disease, Forbes .
Glycogen Debrancher Deficiencies .
Glycogenosis 3s .
Limit Dextrinoses .
Cori's Disease .
Debrancher Deficiency .
Forbes Disease .
Glycogen Debranching Enzyme Deficiency .
Glycogenosis 3 .
Limit Dextrinosis .
An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent. .
0.49
1331
 
Arthritis, Juvenile .
Enthesitis-Related Arthritis, Juvenile .
Juvenile Chronic Arthritis .
Juvenile Idiopathic Arthritis .
Juvenile Rheumatoid Arthritis .
Juvenile-Onset Still Disease .
Juvenile-Onset Stills Disease .
Oligoarthritis, Juvenile .
Polyarthritis, Juvenile, Rheumatoid Factor Negative .
Polyarthritis, Juvenile, Rheumatoid Factor Positive .
Psoriatic Arthritis, Juvenile .
Still Disease, Juvenile-Onset .
Systemic Arthritis, Juvenile .
Arthritis, Juvenile Enthesitis-Related .
Arthritis, Juvenile Psoriatic .
Arthritis, Juvenile Systemic .
Chronic Arthritis, Juvenile .
Enthesitis Related Arthritis, Juvenile .
Idiopathic Arthritis, Juvenile .
Juvenile Arthritis .
Juvenile Enthesitis-Related Arthritis .
Juvenile Oligoarthritis .
Juvenile Onset Still Disease .
Juvenile Onset Stills Disease .
Juvenile Psoriatic Arthritis .
Juvenile Systemic Arthritis .
Juvenile-Onset Still's Disease .
Rheumatoid Arthritis, Juvenile .
Still Disease, Juvenile Onset .
Still's Disease, Juvenile Onset .
Stills Disease, Juvenile-Onset .
Arthritis, Juvenile Chronic .
Arthritis, Juvenile Idiopathic .
Arthritis, Juvenile Rheumatoid .
Still's Disease, Juvenile-Onset .
STILL'S DISEASE .
Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. .
0.48
3439122