acidosis, lactic

Preferred Label : acidosis, lactic;

MeSH definition : Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE.;

MeSH synonym : lactic acidosis;

MeSH annotation : accumulation of lactic acid;

Wikipedia link : https://en.wikipedia.org/wiki/Lactic acidosis;

Details

Origin ID

D000140;

UMLS CUI

C0001125;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Acidosis [ICD-10 Sub-category]
- Acidosis [ICD-10 Sub-category (who)]
- Hyperlactacidemia [PASCAL descriptor]
DO Cross reference
- lactic acidosis [DO Concept]
HPO term
- Lactic acidosis [HPO term]
Record concept(s)
- acidosis, lactic [MeSH concept]
Related MeSH Supplementary Concept(s)
- combined oxidative phosphorylation deficiency 2 [MeSH Supplementary Concept]
- combined oxidative phosphorylation deficiency 3 [MeSH Supplementary Concept]
- combined oxidative phosphorylation deficiency 4 [MeSH Supplementary Concept]
- finnish lethal neonatal metabolic syndrome [MeSH Supplementary Concept]
- lactic acidosis congenital infantile [MeSH Supplementary Concept]
- lactic acidosis, chronic adult form [MeSH Supplementary Concept]
- lactic acidosis, congenital infantile, due to LAD deficiency [MeSH Supplementary Concept]
- lactic acidosis, fatal infantile [MeSH Supplementary Concept]
- maple syrup urine disease, E3 deficient, with lactic acidosis [MeSH Supplementary Concept]
- mitochondrial myopathy with lactic acidosis [MeSH Supplementary Concept]
- myopathy with lactic acidosis, hereditary [MeSH Supplementary Concept]
- pyruvate dehydrogenase E1 alpha deficiency [MeSH Supplementary Concept]
- pyruvate dehydrogenase E2 deficiency [MeSH Supplementary Concept]
- pyruvate dehydrogenase E3-Binding protein deficiency [MeSH Supplementary Concept]
- pyruvate dehydrogenase phosphatase deficiency [MeSH Supplementary Concept]
- tricarboxylic acid cycle, defect of [MeSH Supplementary Concept]
See also
- Hyperlactatemia [MeSH Descriptor]
See also (suggested by CISMeF)
- Hyperlactatemia [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ACIDOSIS LACTIC [WHO-ART Preferred Term]
- Acidosis lactic [MedDRA LLT]
- Lactic Acidosis [NCIt concept]
- Lactic acidosis [MedDRA Preferred Term]
- Lactic acidosis [HPO term]
- Lactic acidosis (disorder) [SNOMED CT concept]
- lactic acidosis [SNOMED Notion]
- lactic acidosis [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients