combined malonic and methylmalonic acidemia

Summary
Synonym
  • CMAMMA
  • combined malonic and methylmalonic aciduria
Definition
An organic acidemia characterized by elevated levels of methylmalonic acid and malonic acid in body fluids typically resulting in developmental delay and failure to thrive in children and neurological symptoms in adults that has_material_basis_in homozygous or compound heterozygous mutation in ACSF3 on 16q24.3.
Super Class
autosomal recessive disease organic acidemia
External Links
Disease Ontology
DOID:0111263
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
197322 ACSF3 acyl-CoA synthetase family member 3
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q4G176 Malonate--CoA ligase ACSF3, mitochondrial
The Human Phenotype Ontology
Displaying entries 21 - 25 of 25 in total
HPO ID HPO Term
HP:0000750 Delayed speech and language development
HP:0002912 Methylmalonic acidemia
HP:0001944 Dehydration
HP:0000007 Autosomal recessive inheritance
HP:0002014 Diarrhea
Displaying 1 entry
Gene ID Gene Symbol Description
197322 ACSF3 acyl-CoA synthetase family member 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024