Increased total bilirubin
Symptom Information:
Symptom ID: | HPO:0003573 | |||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Increased total bilirubin(HPO:0003573) MedDRA: |
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Database Frequency: | 10 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Biliary atresia | (Orphanet:30391) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Glycogen storage disease due to muscle phosphofructokinase deficiency | (Orphanet:371) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
Isolated polycystic liver disease | (Orphanet:2924) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |