serw-MX  [xml]  
 


    
 DeCS Categories

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 .
C10.228.140.163.100.355 Hartnup Disease .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.885 Renal Aminoacidurias .
C12.777.419.815.885.457 Hartnup 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 .
C13.351.968.419.815.885 Renal Aminoacidurias .
C13.351.968.419.815.885.625 Hartnup Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.151 Amino Acid Transport Disorders, Inborn .
C16.320.565.151.355 Hartnup Disease .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.355 Hartnup Disease .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.885 Renal Aminoacidurias .
C16.320.565.861.885.457 Hartnup Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.355 Hartnup Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.151 Amino Acid Transport Disorders, Inborn .
C18.452.648.151.355 Hartnup Disease .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.355 Hartnup Disease .
D12 Amino Acids, Peptides, and Proteins .
D12.125 Amino Acids .
D12.125.067 Amino Acids, Acidic .
D12.125.154 Amino Acids, Neutral .
D12.776 Proteins .
D12.776.157 Carrier Proteins .
D12.776.157.530 Membrane Transport Proteins .
D12.776.157.530.200 Amino Acid Transport Systems .
D12.776.157.530.200.500 Amino Acid Transport Systems, Neutral .
D12.776.543 Membrane Proteins .
D12.776.543.585 Membrane Transport Proteins .
D12.776.543.585.200 Amino Acid Transport Systems .
D12.776.543.585.200.500 Amino Acid Transport Systems, Neutral .
SP4 Environmental Health .
SP4.011 Science .
SP4.011.097 Chemistry .
SP4.011.097.036 Organic Chemicals .
SP4.011.097.036.604 Amines .
SP4.011.097.036.604.345 Amino Acids .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Amino Acids, Neutral .
Acids, Neutral Amino .
Neutral Amino Acids .
Amino acids with uncharged R groups or side chains. .
1.00
1241
 
Amino Acids .
Acids, Amino .
Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins. .
0.76
463118337
 
Amino Acid Transport Systems, Neutral .
Na+-Independent Neutral Amino Acid Transporter .
Neutral Amino Acid Transport Proteins .
Sodium Dependent Neutral Amino Acid Transport Proteins .
Sodium Dependent Neutral Amino Acid Transporters .
Sodium Independent Neutral Amino Acid Transport Proteins .
Sodium Independent Neutral Amino Acid Transporters .
Zwitterionic Amino Acid Transport Proteins .
Zwitterionic Amino Acid Transporters .
Na+ Independent Neutral Amino Acid Transporter .
Neutral Amino Acid Transport Systems .
Neutral Amino Acid Transporters .
Zwitterionic Amino Acid Transport Systems .
Amino acid transporter systems capable of transporting neutral amino acids (AMINO ACIDS, NEUTRAL). .
0.75
11134
 
Amino Acids, Acidic .
Amino Acid, Acidic .
Acidic Amino Acid .
Acidic Amino Acids .
Amino acids with side chains that are negatively charged at physiological pH. .
0.71
1158
 
Hartnup Disease .
Hartnup Disorder .
Neutral Amino Acid Transport Defect .
Transport Disorder, Neutral Amino Acids .
Amino Acid Transport Disorder, Neutral .
Neutral Amino Acid Transport Disorder .
Transport Disorder, Neutral Amino Acid .
An autosomal recessive disorder due to defective absorption of NEUTRAL AMINO ACIDS by both the intestine and the PROXIMAL RENAL TUBULES. The abnormal urinary loss of TRYPTOPHAN, a precursor of NIACIN, leads to a NICOTINAMIDE deficiency, PELLAGRA-like light-sensitive rash, CEREBELLAR ATAXIA, emotional instability, and aminoaciduria. Mutations involve the neurotransmitter transporter gene SLC6A19. .
0.71
2225