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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
metabolic disease +     
acquired metabolic disease +   
ALG13-CDG 
amino acid metabolism disease +   
amino-acid transport disorder 
Autism spectrum disorder-epilepsy-arthrogryposis syndrome 
Autosomal dominant primary hypomagnesemia with hypocalciuria 
Autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency 
bilirubin metabolism disease +   
carbohydrate metabolism disease +   
chondrocalcinosis +  
CHST3-related skeletal dysplasia 
Chédiak-Higashi syndrome 
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome 
Congenital atransferrinemia 
Congenital dyserythropoietic anemia type II 
Congenital muscular dystrophy, Fukuyama type 
developmental anomaly of metabolic origin +  
diabetic nephropathy +   
diabetic retinopathy +   
disorder of acid-base balance +   
Disorder of amino acid and other organic acid metabolism +  
Disorder of biogenic amine metabolism and transport +  
Disorder of carbohydrate metabolism +  
Disorder of energy metabolism +  
Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation +  
disorder of glycosylation +  
Disorder of lipid metabolism +   
disorder of organic acid metabolism +  
Disorder of porphyrin and haem metabolism +  
Disorder of purine or pyrimidine metabolism +   
Disorder of vitamin and non-protein cofactor absorption and transport  +  
Distal myopathy, Nonaka type 
dopa-responsive dystonia +  
DPM1-CDG 
Ehlers-Danlos syndrome, progeroid type 
FTH1-related iron overload 
glucose metabolism disease +   
glutaric aciduria +  
gout +   
hemochromatosis 
hepatic methionine adenosyltransferase deficiency 
hyperamylasemia 
hyperlipidemia +   
hyperlipoproteinemia +   
hyperprolactinemia +  
Hypertriglyceridemia +   
hypoalphalipoproteinemia +  
inborn errors of metabolism +   
lactic acidosis +  
lipodystrophy +  
Lysosomal disease +  
metabolic syndrome  
A cluster of metabolic risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome X include excess ABDOMINAL FAT; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. (from AHA/NHLBI/ADA Conference Proceedings, Circulation 2004; 109:551-556)
metabolic toxicity 
methylmalonic aciduria (cobalamin deficiency) cblA type 
mineral metabolism disease +   
muscular dystrophy, congenital, with cataracts and intellectual disability 
nutritional disorder +   
Other metabolic disease +  
Papillon-Lefèvre syndrome 
Peroxisomal beta-oxidation disorder +  
peroxisome biogenesis disorder, complementation group 7 
Peroxisome biogenesis disorder-Zellweger syndrome spectrum +  
porphyrin metabolism disease +  
Primary hypomagnesemia with secondary hypocalcemia 
proteostasis deficiencies +   
purine metabolism disease +  
pyrimidine metabolism disease +  
Rare hereditary hemochromatosis 
Recurrent infections - inflammatory syndrome due to zinc metabolism disorder 
Refsum disease 
steroid dehydrogenase deficiency-dental anomalies syndrome 
steroid metabolism disease +  
Tumor Lysis Syndrome 
x-linked warfarin sensitivity 
xanthinuria +  
xanthoma 

Synonyms
Exact Synonyms: Cardiovascular Syndromes, Metabolic ;   Dysmetabolic Syndrome X ;   Insulin Resistance Syndrome X ;   MetS ;   Metabolic Cardiovascular Syndrome ;   Metabolic Syndrome X ;   Reaven Syndrome X
Xrefs: DOID:14221 ;   DOID:9006646 ;   ICD9:277.7 ;   MESH:D024821 ;   MIM:605552 ;   MIM:615812 ;   MedDRA:10052066 ;   NCI:C84442 ;   SNOMEDCT:237602007

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