Hyperbilirubinemia
Symptom Information:
| Symptom ID: | HPO:0002904 | ||
| Synonyms: |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Hyperbilirubinemia(HPO:0002904) MedDRA: |
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| Database Frequency: | 32 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
| BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4 | (OMIM:214950) |
| BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 | (OMIM:601816) |
| Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
| Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
| Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
| Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
| Congenital dyserythropoietic anemia type IV | (Orphanet:293825) |
| Gaucher disease type 2 | (Orphanet:77260) |
| HYPERBILIRUBINEMIA, SHUNT, PRIMARY | (OMIM:237800) |
| Hemochromatosis type 3 | (Orphanet:225123) |
| Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
| Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
| Hereditary fructose intolerance | (Orphanet:469) |
| Hereditary spherocytosis | (Orphanet:822) |
| Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
| Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
| Lathosterolosis | (Orphanet:46059) |
| Leprechaunism | (Orphanet:508) |
| MEGDEL syndrome | (Orphanet:352328) |
| MITCHELL-RILEY SYNDROME | (OMIM:615710) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
| Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
| Nephronophthisis 9 | (OMIM:613824) |
| Non-spherocytic hemolytic anemia due to hexokinase deficiency | (Orphanet:90031) |
| PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
| RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS | (OMIM:179700) |
| Reynolds syndrome | (Orphanet:779) |
| SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1 | (OMIM:109270) |
| SPECTRIN, BETA, ERYTHROCYTIC | (OMIM:182870) |
| SPHEROCYTOSIS, TYPE 1 | (OMIM:182900) |
| Thyroid ectopia | (Orphanet:95712) |