UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M M0 M1 M2 M4 M5 M7 M8 M9 MA MB MC MD ME MF MG MH MI MK ML MM MN MO MP MR MS MT MU MV MY
ME ME ME2 MEA MEB MEC MED MEE MEF MEG MEI MEL MEM MEN MEP MEQ MER MES MET MEV MEX MEZ

Metabolic Disease

[condition in which there is a deviation from or caused by an abnormal metabolic process; can be congenital due to inherited enzyme abnormality (INBORN METABOLISM DISORDER) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. ( CSP )]
UMLS (NCI) C0025517
 
Disease or Syndrome
Relation/PAR: Disease
Nutritional and Metabolic Diseases
Relation/CHD: acidosis
alkalosis
amyloid disease
Bone Diseases, Metabolic
Diabete mellito
histiocytosis X
hyperbilirubinemia
Congenital Metabolic Disorder
DIS PHOSPHORUS METABOL
DIS PORPHYRIN METABOLISM
Alteracoes do metabolismo lipidico
steroid metabolism disorder
FLUID OVERLOAD
hypovolemia
acquired aminoacid metabolism disorder
metal metabolism disorder
protein metabolism disorder
hyperuricemia
mitochondrial disease
achlorhydria
Acid-Base Imbalance
Brain Diseases, Metabolic
calcium metabolism disorder
diabetes insipidus
Diabete mellito
DIS IRON METABOLISM
glycosuria
hyperbilirubinemia
Blood Glucose, High
hyperinsulinemia
hyperlipemia
hyperprolactinemia
HYPERVITAMINOSIS A
Blood Glucose, Low
gastrointestinal absorption disorder
Congenital Metabolic Disorder
DIS PHOSPHORUS METABOL
Protein-Losing Enteropathies
Wasting Syndrome
Water-Electrolyte Imbalance
xanthelasmatosis
enzyme deficiency
Hyperammonemia
hyperuricemia

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