Cytoscape Web
Click node...

Transient familial neonatal hyperbilirubinemia
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Crigler-Najjar syndrome type 1
Crigler-Najjar syndrome type 2
Congenital dyserythropoietic anemia type II
Synonym(s):
- Lucey-Driscoll syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
UGT1A1 P22309191740
No signs/symptoms info available.