Preferred Label : methylmalonic acid;

MeSH definition : A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.;

MeSH synonym : acid, methylmalonic;

MeSH CAS label : propanedioic acid, methyl-;

MeSH Related Number : 516-05-2 (Methylmalonic acid);

Registry Number MeSH : 516-05-2;

MeSH annotation : /biosyn /physiol permitted;

Wikipedia link : https://en.wikipedia.org/wiki/Methylmalonic acid;

Codes EINECS : 208-219-5;

Is substance : O;

UNII : 8LL8S712J7;

InChIKey : ZIYVHBGGAOATLY-UHFFFAOYSA-N;

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A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.

https://www.has-sante.fr/jcms/p_3192841/fr/aciduries-organiques-acidemie-methylmalonique-et-acidemie-propionique
2020
France
practice guideline
organizations
Acidemia
organ part
methylmalonic acidemia
propionicaciduria
Handbook
methylmalonic acid
chronic disease, nos
Organism
chronic disease
Methylmalonic Aciduria
Organisms Category
propionic acidemia, nos
Chronic disease
propionic acidemia
Aciduria
Diseases
methylmalonic acidemia, nos
aciduria
organizations
Handbook
amino acid metabolism, inborn errors

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https://www.anses.fr/fr/system/files/NUT2016SA0021.pdf
2017
false
false
false
France
French
scientific and technical information
propionic acid
nutrition therapy
judgment
nutritional requirement
propionic acids
child, nos
methylmalonic acidemia, nos
Amino acid
propionic acid
needs
inlets
methylmalonic acid
relative
medical
propionic acidemia, nos
treaties
nutritional disorder, nos
hereditary disease, nos
nutritional and metabolic diseases
metabolic disease, nos
nutritional requirements
special
methylmalonic acidemia
has assessment
specialists
hereditary diseases
amino acids
amino acid, nos
child
propionic acidemia
propionates
health services needs and demand
bays
international cooperation
nutritional and metabolic diseases
evaluation studies as topic
specialization
genetic diseases, inborn
amino acid metabolism, inborn errors

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=28
2012
true
France
French
scientific and technical information
methylmalonic acid

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=17
2006
France
French
scientific and technical information
acidosis, lactic
acidosis, lactic
child
rare diseases
lactic acidosis congenital infantile
signs and symptoms
methylmalonic acid

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24/05/2025


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