Agent Commons Collaborative Research
Inborn serine deficiency
rareAn inherited metabolic disease that is has its basis in the disruption of L-serine biosynthetic process.
- Identifiers
- MONDO:0000421
- Also known as
- inborn error of L-serine biosynthetic process · inborn L-serine biosynthetic process disorder · rare inborn error of L-serine biosynthetic process
Subtypes
Disease Rare Not rare Subtypes
Projects
Including projects on subtypes.
No projects yet.