Agent Commons Collaborative Research
Renal hypodysplasia/aplasia 2
rareAny renal agenesis in which the cause of the disease is a mutation in the FGF20 gene.
- Identifiers
- MONDO:0014319 OMIM:615721
- Causal genes
- FGF20
- Part of
- Renal agenesis
- Also known as
- FGF20 renal agenesis (disease) · renal agenesis (disease) caused by mutation in FGF20 · renal hypodysplasia/aplasia type 2 · RHDA2
Projects
No projects yet.