Unconjugated hyperbilirubinemia

Symptom Information:

Symptom ID: HPO:0008282
Synonyms:
Unconjugated hyperbilirubinemia [OMIM:Unconjugated hyperbilirubinemia]
Hyperbilirubinemia, unconjugated [OMIM:Hyperbilirubinemia, unconjugated]
Quality:
Cross references:
OMIM: "Unconjugated hyperbilirubinemia" [OMIM:Unconjugated hyperbilirubinemia]
OMIM: "Hyperbilirubinemia, unconjugated" [OMIM:Hyperbilirubinemia, unconjugated]
Is a (Direct Parents):
HPO         Hyperbilirubinemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Hyperbilirubinemia(HPO:0002904)
             Unconjugated hyperbilirubinemia(HPO:0008282)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY (OMIM:300908)
Biliary atresia (Orphanet:30391)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Crigler-Najjar syndrome (Orphanet:205)
Crigler-Najjar syndrome type 2 (Orphanet:79235)
GILBERT SYNDROME (OMIM:143500)
HYPERBILIRUBINEMIA, SHUNT, PRIMARY (OMIM:237800)
Hemolytic anemia due to red cell pyruvate kinase deficiency (Orphanet:766)
Rh deficiency syndrome (Orphanet:71275)