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 DeCS Categories

C02 Virus Diseases .
C02.782 RNA Virus Infections .
C02.782.687 Picornaviridae Infections .
C02.782.687.359 Enterovirus Infections .
C02.782.687.359.456 Encephalomyelitis, Enzootic Porcine .
C08 Respiratory Tract Diseases .
C08.460 Nose Diseases .
C09 Otorhinolaryngologic Diseases .
C09.603 Nose Diseases .
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 .
C10.228.140.163.100.425 Lesch-Nyhan Syndrome .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.625 Lesch-Nyhan Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.625 Lesch-Nyhan Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.625 Lesch-Nyhan Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.425 Lesch-Nyhan Syndrome .
C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C16.320.565.798.594 Lesch-Nyhan Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.425 Lesch-Nyhan Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.425 Lesch-Nyhan Syndrome .
C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C18.452.648.798.594 Lesch-Nyhan Syndrome .
C22 Animal Diseases .
C22.905 Swine Diseases .
C22.905.323 Encephalomyelitis, Enzootic Porcine .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
D02 Organic Chemicals .
D02.065 Amides .
D02.065.884 Sulfonamides .
D02.065.884.725 Sulfanilamides .
D02.065.884.725.867 Sulfamethoxazole .
D02.065.884.725.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D02.092 Amines .
D02.092.146 Aniline Compounds .
D02.092.146.807 Sulfanilamides .
D02.092.146.807.867 Sulfamethoxazole .
D02.092.146.807.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D02.886 Sulfur Compounds .
D02.886.590 Sulfones .
D02.886.590.700 Sulfonamides .
D02.886.590.700.725 Sulfanilamides .
D02.886.590.700.725.867 Sulfamethoxazole .
D02.886.590.700.725.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.742 Pyrimidines .
D03.383.742.906 Trimethoprim .
D03.383.742.906.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D26 Pharmaceutical Preparations .
D26.310 Drug Combinations .
D26.310.875 Trimethoprim, Sulfamethoxazole Drug Combination .
HP1 Homeopathy .
HP1.007 Homeopathic Philosophy .
HP1.007.262 Patients .
HP1.007.262.808 Disease .
HP2 Homeopathic Clinics .
HP2.029 Disease .
SP5 Epidemiology and Biostatistics .
SP5.001 Epidemiology .
SP5.001.002 Health-Disease Process .
SP5.001.002.013 Disease .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lesch-Nyhan Syndrome .
Choreoathetosis Self-Mutilation Syndrome .
Complete HGPRT Deficiency Disease .
Complete HPRT Deficiency .
Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency .
Deficiency Disease, Complete HGPRT .
Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase .
Deficiency of Guanine Phosphoribosyltransferase .
Deficiency of Hypoxanthine Phosphoribosyltransferase .
HGPRT Deficiency .
HGPRT Deficiency Disease, Complete .
Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency .
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency .
Hypoxanthine Phosphoribosyltransferase Deficiency .
Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome .
Juvenile Hyperuricemia Syndrome .
Lesch-Nyhan Disease .
Primary Hyperuricemia Syndrome .
Total HPRT Deficiency .
Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency .
X-Linked Hyperuricemia .
X-Linked Primary Hyperuricemia .
Choreoathetosis Self Mutilation Hyperuricemia Syndrome .
Choreoathetosis Self Mutilation Syndrome .
Choreoathetosis Self-Mutilation Syndromes .
Complete HPRT Deficiencies .
Complete Hypoxanthine Guanine Phosphoribosyltransferase Deficiency .
Deficiencies, Complete HPRT .
Deficiencies, HGPRT .
Deficiencies, Hypoxanthine Phosphoribosyltransferase .
Deficiencies, Total HPRT .
Deficiency Disease, Hypoxanthine Phosphoribosyl Transferase .
Deficiency Diseases, Hypoxanthine-Phosphoribosyl-Transferase .
Deficiency, Complete HPRT .
Deficiency, HGPRT .
Deficiency, Hypoxanthine Phosphoribosyltransferase .
Deficiency, Total HPRT .
Guanine Phosphoribosyltransferase Deficiencies .
Guanine Phosphoribosyltransferase Deficiency .
HGPRT Deficiencies .
HPRT Deficiencies, Complete .
HPRT Deficiencies, Total .
HPRT Deficiency, Complete .
HPRT Deficiency, Total .
Hyperuricemia Syndrome, Juvenile .
Hyperuricemia Syndrome, Primary .
Hyperuricemia Syndromes, Juvenile .
Hyperuricemia Syndromes, Primary .
Hyperuricemia, X-Linked .
Hyperuricemia, X-Linked Primary .
Hyperuricemias, X-Linked .
Hyperuricemias, X-Linked Primary .
Hypoxanthine Phosphoribosyl Transferase Deficiency Disease .
Hypoxanthine Phosphoribosyltransferase Deficiencies .
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Diseases .
Juvenile Hyperuricemia Syndromes .
Lesch Nyhan Disease .
Lesch Nyhan Syndrome .
Phosphoribosyltransferase Deficiencies, Guanine .
Phosphoribosyltransferase Deficiencies, Hypoxanthine .
Phosphoribosyltransferase Deficiency, Guanine .
Phosphoribosyltransferase Deficiency, Hypoxanthine .
Primary Hyperuricemia Syndromes .
Primary Hyperuricemia, X-Linked .
Primary Hyperuricemias, X-Linked .
Self-Mutilation Syndrome, Choreoathetosis .
Self-Mutilation Syndromes, Choreoathetosis .
Syndrome, Choreoathetosis Self-Mutilation .
Syndrome, Juvenile Hyperuricemia .
Syndrome, Primary Hyperuricemia .
Syndromes, Choreoathetosis Self-Mutilation .
Syndromes, Juvenile Hyperuricemia .
Syndromes, Primary Hyperuricemia .
Total HPRT Deficiencies .
Total Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency .
X Linked Hyperuricemia .
X Linked Primary Hyperuricemia .
X-Linked Hyperuricemias .
X-Linked Primary Hyperuricemias .
Choreoathetosis Self-Mutilation Hyperuricemia Syndrome .
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease .
An inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE. Affected individuals are normal in the first year of life and then develop psychomotor retardation, extrapyramidal movement disorders, progressive spasticity, and seizures. Self-destructive behaviors such as biting of fingers and lips are seen frequently. Intellectual impairment may also occur but is typically not severe. Elevation of uric acid in the serum leads to the development of renal calculi and gouty arthritis. (Menkes, Textbook of Child Neurology, 5th ed, pp127) .
1.00
201179
 
Disease .
Diseases .
Illness .
Disease Concept Evolution .
A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. .
0.45
93917203
 
Encephalomyelitis, Enzootic Porcine .
Porcine Poliomyelitis .
Disease, Talfan .
Disease, Teschen .
Enzootic Porcine Encephalomyelitis .
Porcine Encephalomyelitis, Enzootic .
Talfan Disease .
Teschen Disease .
Poliomyelitis, Porcine .
A picornavirus infection producing symptoms similar to poliomyelitis in pigs. .
0.40
 
Trimethoprim, Sulfamethoxazole Drug Combination .
Abactrim .
Bactifor .
Bactrim .
Biseptol .
Biseptol-480 .
Centran .
Centrin .
Co-Trimoxazole .
Cotrimoxazole .
Drylin .
Eslectin .
Eusaprim .
Insozalin .
Kepinol .
Kepinol Forte .
Lescot .
Metomide .
Oriprim .
Septra .
Septrin .
Sulfamethoxazole-Trimethoprim Combination .
Sulprim .
Sumetrolim .
TMP SMX .
TMP-SMX .
Trimedin .
Trimethoprim-Sulfamethoxazole .
Trimethoprimsulfa .
Trimezole .
Trimosulfa .
Biseptol 480 .
Biseptol480 .
Co Trimoxazole .
Sulfamethoxazole Trimethoprim Combination .
Trimethoprim Sulfamethoxazole .
Trimethoprim Sulfamethoxazole Combination .
Cotrimoxazole .
Trimethoprim-Sulfamethoxazole Combination .
Trimethoprim, Sulfamethoxazole Combination .
A drug combination with broad-spectrum antibacterial activity against both gram-positive and gram-negative organisms. It is effective in the treatment of many infections, including PNEUMOCYSTIS PNEUMONIA in AIDS. .
0.39
2376387
 
Nose Diseases .
Nasal Disorders .
Disease, Nasal .
Disease, Nose .
Diseases, Nasal .
Diseases, Nose .
Disorder, Nasal .
Disorders, Nasal .
Nasal Disease .
Nasal Disorder .
Nose Disease .
Nasal Diseases .
Disorders of the nose, general or unspecified. .
0.38
1324884