Disease #01852

Official abbreviation HBLRTFN
Name hyperbilirubinemia, familial transient neonatal (Lucey-Driscoll syndrome (HBLRTFN))
OMIM ID 237900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UGT1A1
Associated tissues -
Disease features -
Remarks -