Unconjugated hyperbilirubinemia
Symptom Information:
Symptom ID: | HPO:0008282 | ||
Synonyms: |
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Cross references: |
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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: |
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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) |