Conjugated hyperbilirubinemia
Symptom Information:
Symptom ID: | HPO:0002908 | ||||
Synonyms: |
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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) Conjugated hyperbilirubinemia(HPO:0002908) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||
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All diseases associated with this symptom:
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY | (OMIM:210550) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Benign recurrent intrahepatic cholestasis type 1 | (Orphanet:99960) |
Benign recurrent intrahepatic cholestasis type 2 | (Orphanet:99961) |
Cholestasis - lymphedema | (Orphanet:1414) |
Dubin-Johnson syndrome | (Orphanet:234) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
HYPERBILIRUBINEMIA, CONJUGATED, TYPE III | (OMIM:237550) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Jeune syndrome | (Orphanet:474) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Progressive familial intrahepatic cholestasis type 1 | (Orphanet:79306) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
Rotor syndrome | (Orphanet:3111) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |