| MeSH term | MeSH ID | Detail |
|---|---|---|
| Metabolism, Inborn Errors | D008661 | 46 associated lipids |
Total
1
5-hydroxyhexanoic acid
5-hydroxyhexanoic 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 50 references associated with 5-hydroxyhexanoic 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 5-hydroxyhexanoic acid
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with 5-hydroxyhexanoic acid
PubChem Associated disorders and diseases
NCBI Entrez Crosslinks
All references with 5-hydroxyhexanoic acid
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Woo HI et al. | Clinical, biochemical and genetic analyses in two Korean patients with medium-chain acyl-CoA dehydrogenase deficiency. | 2011 | Korean J Lab Med | pmid:21239873 |
| Dessein AF et al. | A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report. | 2010 | Orphanet J Rare Dis | pmid:20923556 |
| Boulat O et al. | Organic acids in the second morning urine in a healthy Swiss paediatric population. | 2003 | Clin. Chem. Lab. Med. | pmid:14708889 |
| Tserng KY et al. | Distinction of dicarboxylic aciduria due to medium-chain triglyceride feeding from that due to abnormal fatty acid oxidation and fasting in children. | 1996 | Metab. Clin. Exp. | pmid:8596483 |
| Loftus NJ et al. | Metabolism and pharmacokinetics of deuterium-labelled di-2-(ethylhexyl) adipate (DEHA) in humans. | 1993 | Food Chem. Toxicol. | pmid:8406236 |
| Brass EP et al. | Urinary organic acid excretion during feeding of medium-chain or long-chain triglyceride diets in patients with non-insulin-dependent diabetes mellitus. | 1990 | Am. J. Clin. Nutr. | pmid:2239769 |
| Colle E et al. | Episodic hypoglycemia with psi-hydroxy fatty acid excretion. | 1983 | Pediatr. Res. | pmid:6402754 |
| Kamerling JP et al. | The absolute configuration of urinary 5-hydroxyhexanoic acid - a product of fatty acid (omega-1)-oxidation - in patients with non-ketotic dicarboxylic aciduria. | 1982 | Clin. Chim. Acta | pmid:6897376 |
| Gregersen N et al. | Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases. | 1980 | Clin. Chim. Acta | pmid:6892795 |
| Mamer OA et al. | Profiles in altered metabolism. II--(omega -- 1)-hydroxyacid excretion in a case of episodic hypoglycemia. | 1980 | Biomed. Mass Spectrom. | pmid:6893290 |