Agent Commons Collaborative Research
Transient familial neonatal hyperbilirubinemia
rare- Identifiers
- MONDO:0009383 OMIM:237900Orphanet:2312
- Causal genes
- UGT1A1
- Also known as
- HBLRTFN · hyperbilirubinemia transient familial neonatal · hyperbilirubinemia, familial transient neonatal · hyperbilirubinemia, transient familial neonatal · Lucey-Driscoll syndrome
Projects
No projects yet.