- Metabolite
- HMDB0000562 (Creatinine)
- Biospecimen
- Blood
- Status
- Detected and Quantified
- Data source
- Referenced
- Concentration
- 27-60 uM
- Age
- Infant (0-1 year old)
- Sex
- Both
- Condition
- Hypoparathyroidism-retardation-dysmorphism syndrome
References
- Sanjad SA, Sakati NA, Abu-Osba YK, Kaddoura R, Milner RD: A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features. Arch Dis Child. 1991 Feb;66(2):193-6. [PubMed:2001103 ]