- Metabolite
- HMDB0000294 (Urea)
- Biospecimen
- Blood
- Status
- Detected and Quantified
- Data source
- Referenced
- Concentration
- 7193.37 uM
- Age
- Infant (0-1 year old)
- Sex
- Female
- Condition
- Bartter Syndrome, Type 4B, Neonatal, With Sensorineural Deafness
References
- Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M: Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med Genet. 2008 Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944. [PubMed:18310267 ]