| 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 |
|---|---|---|---|---|
| Thompson WR et al. | New targets for monitoring and therapy in Barth syndrome. | 2016 | Genet. Med. | pmid:26845103 |
| Su B and Ryan RO | Metabolic biology of 3-methylglutaconic acid-uria: a new perspective. | 2014 | J. Inherit. Metab. Dis. | pmid:24407466 |
| Santarelli F et al. | A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency. | 2013 | Ital J Pediatr | pmid:23705938 |
| Wortmann SB et al. | Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. | 2013 | J. Inherit. Metab. Dis. | pmid:23296368 |
| Wortmann SB et al. | 3-Methylglutaconic aciduria--lessons from 50 genes and 977 patients. | 2013 | J. Inherit. Metab. Dis. | pmid:23355087 |
| Wortmann SB et al. | The 3-methylglutaconic acidurias: what's new? | 2012 | J. Inherit. Metab. Dis. | pmid:20882351 |
| Roullet JB et al. | No evidence for mevalonate shunting in moderately affected children with Smith-Lemli-Opitz syndrome. | 2012 | J. Inherit. Metab. Dis. | pmid:22391996 |
| Bekheirnia MR et al. | POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria. | 2012 | Gene | pmid:22405928 |
| Ronvelia D et al. | Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. | 2012 | Mol. Genet. Metab. | pmid:23031367 |
| Tort F et al. | Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria. | 2011 | Clin. Genet. | pmid:21815885 |