MeSH term | MeSH ID | Detail |
---|---|---|
Metabolism, Inborn Errors | D008661 | 46 associated lipids |
Total
1
5-hydroxyhexanoic acid is a lipid of Fatty Acyls (FA) class.
We collected disease MeSH terms mapped to the references associated with 5-hydroxyhexanoic acid
MeSH term | MeSH ID | Detail |
---|---|---|
Metabolism, Inborn Errors | D008661 | 46 associated lipids |
Authors | Title | Published | Journal | PubMed Link |
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pmid: | ||||
Boulat O et al. | Organic acids in the second morning urine in a healthy Swiss paediatric population. | 2003 | Clin. Chem. Lab. Med. | pmid:14708889 |
pmid:18231816 | ||||
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 |
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 |
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 |
pmid:22998979 | ||||
pmid:27352185 | ||||
Lawson AM and Chalmers RA | Identification of 5-hydroxyhexanoic acid in the urine of twin siblings with a syndrome having close similarities to Jamaican vomiting sickness [proceedings]. | 1978 | Biochem. Soc. Trans. | pmid:640132 |
Colle E et al. | Episodic hypoglycemia with psi-hydroxy fatty acid excretion. | 1983 | Pediatr. Res. | pmid:6402754 |