Conjugated hyperbilirubinemia

Symptom Information:

Symptom ID: HPO:0002908
Synonyms:
Direct hyperbilirubinemia [HPO:0002908]
Conjugated hyperbilirubinemia [OMIM:Conjugated hyperbilirubinemia]
Hyperbilirubinemia, conjugated [OMIM:Hyperbilirubinemia, conjugated]
Hyperbilirubinemia, direct [OMIM:Hyperbilirubinemia, direct]
Quality:
Cross references:
OMIM: "Conjugated hyperbilirubinemia" [OMIM:Conjugated hyperbilirubinemia]
OMIM: "Hyperbilirubinemia, conjugated" [OMIM:Hyperbilirubinemia, conjugated]
OMIM: "Hyperbilirubinemia, direct" [OMIM:Hyperbilirubinemia, direct]
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)
             Conjugated hyperbilirubinemia(HPO:0002908)
MedDRA:
Database Frequency: 21 / 7739
Resource:

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)