| MeSH term | MeSH ID | Detail |
|---|---|---|
| Acidosis, Lactic | D000140 | 8 associated lipids |
| Liver Diseases | D008107 | 31 associated lipids |
| Quadriplegia | D011782 | 4 associated lipids |
| Abnormalities, Multiple | D000015 | 13 associated lipids |
| Intellectual Disability | D008607 | 13 associated lipids |
| Metabolism, Inborn Errors | D008661 | 46 associated lipids |
| Acidosis, Renal Tubular | D000141 | 4 associated lipids |
| Brain Diseases, Metabolic, Inborn | D020739 | 10 associated lipids |
| Cardiomyopathies | D009202 | 10 associated lipids |
| Neutropenia | D009503 | 15 associated lipids |
3E-methylglutaconic acid
3e-methylglutaconic acid is a lipid of Fatty Acyls (FA) class.
Cross Reference
There are no associated biomedical information in the current reference collection.
Current reference collection contains 473 references associated with 3E-methylglutaconic acid in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.
Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.
Here are additional resources we collected from PubChem and MeSH for 3E-methylglutaconic acid
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with 3E-methylglutaconic acid
PubChem Associated disorders and diseases
All references with 3E-methylglutaconic acid
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Ly TB et al. | Mutations in the AUH gene cause 3-methylglutaconic aciduria type I. | 2003 | Hum. Mutat. | pmid:12655555 |
| Laube GF et al. | Nephrocalcinosis and medullary cysts in 3-methylglutaconic aciduria. | 2003 | Pediatr. Nephrol. | pmid:12750979 |
| Schlame M et al. | Phospholipid abnormalities in children with Barth syndrome. | 2003 | J. Am. Coll. Cardiol. | pmid:14662265 |
| Rugolotto S et al. | Long-term treatment of Barth syndrome with pantothenic acid: a retrospective study. | 2003 | Mol. Genet. Metab. | pmid:14654353 |
| Kleta R et al. | 3-Methylglutaconic aciduria type III in a non-Iraqi-Jewish kindred: clinical and molecular findings. | 2002 | Mol. Genet. Metab. | pmid:12126933 |
| Sakamoto O et al. | Novel missense mutation (R94S) in the TAZ ( G4.5) gene in a Japanese patient with Barth syndrome. | 2002 | J. Hum. Genet. | pmid:12032589 |
| Scaglia F et al. | Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism. | 2002 | BMC Pediatr | pmid:12507404 |
| Anikster Y et al. | Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews. | 2001 | Am. J. Hum. Genet. | pmid:11668429 |
| Mazzocco MM and Kelley RI | Preliminary evidence for a cognitive phenotype in Barth syndrome. | 2001 | Am. J. Med. Genet. | pmid:11503166 |
| Scaglia F et al. | Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria. | 2001 | J. Child Neurol. | pmid:11292221 |