MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
expandmetabolic disease (MONDO:0005066)
..Starting node
..expandlactic acidosis ()

       Child Nodes:
........expandacquired lactic acidosis ()
........expandcardiomyopathy-hypotonia-lactic acidosis syndrome ()  LSDB  L: 00040;
........expandmitochondrial DNA depletion syndrome 9 ()  LSDB  L: 00038;



 Sister Nodes: 
..expandacquired metabolic disease ()
..expandbilirubin metabolism disease ()
..expandcarbohydrate metabolism disease ()
..expandcarotenemia ()
..expandchondrocalcinosis ()
..expandcomplement deficiency ()
..expanddevelopmental anomaly of metabolic origin ()
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..expanddiabetic retinopathy ()
..expanddisorder of acid-base balance ()
..expanddisorder of glycosylation ()
..expanddisorder of organic acid metabolism ()
..expandDNA repair disease ()
..expandfamilial thyroid dyshormonogenesis ()
..expandglucose metabolism disease ()
..expandglutaric aciduria (disease) ()
..expandgout ()
..expandhemolytic anemia due to an erythrocyte nucleotide metabolism disorder ()
..expandhyperlipidemia (disease) ()
..expandhyperlipoproteinemia ()
..expandhypermanganesemia with dystonia ()
..expandhypertriglyceridemia (disease) ()
..expandhypoalphalipoproteinemia ()
..expandinborn errors of metabolism ()
..expandlactic acidosis ()
..expandlipodystrophy (disease) ()
..expandmetabolic disease with epilepsy ()
..expandmetabolic disease with intestinal involvement ()
..expandmetabolic disease with skin involvement ()
..expandmetabolic syndrome ()
..expandmineral metabolism disease ()
..expandporphyrin metabolism disease ()
..expandproteostasis deficiencies ()
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..expandpyrimidine metabolism disease ()
..expandsteroid metabolism disease ()
..expandthiopurine metabolic disease ()
..expandvitamin B12 deficiency ()
..expandxanthinuria ()
..expandxanthoma (disease) ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:6040
Name:lactic acidosis
Definition:Metabolic acidosis characterized by the accumulation of lactate in the body. It is caused by tissue hypoxia.
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TreeNumbers:
Synonyms:
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Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: TBCE;
Phenotypes
Disease Causing ClinVar Variants
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