Idiopathic ductopenia




Input patient's signs and symptoms


Narrow down the case reports



Total: 5 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(4.0%)
15307528
[Benign form of idiopathic biliary ductopenia in an adult woman].
Hartleb M, Nowak A, Gabriel A.
Wiad Lek. 2004;57(3-4):171-3.
Hypothyroidism
Adult Cholangitis, Sclerosing Differential Diagnosis Females Homo sapiens Intrahepatic Cholestasis
1
(4.0%)
10761970
Idiopathic adulthood ductopenia: case report and review of the literature.
Khanlou H, Sass D, Rothstein K, Manzarbeitia C, Reich D, Jacobson L, Fleischer D, Munoz SJ.
Arch Intern Med. 2000;160(7):1033-6.
Jaundice
Adult Females Homo sapiens Intrahepatic Cholestasis Pruritus
1
(4.0%)
9762195
[Adult idiopathic ductopenia. 1 case].
Brazier F, Duchmann JC, Sevestre H, Capron D, Capron JP.
Gastroenterol Clin Biol. 1998;22(2):227-31.
Jaundice
Adult Bile Duct Diseases Histiocytes Homo sapiens Liver Cirrhosis Lymphocyte Male
1
(4.0%)
9503746
[Idiopathic ductopenia in adults as a cause of cryptogenic cirrhosis and complications of portal hypertension].
Rodriguez Martinez D, Fernandez Rodriguez CM, Rodriguez Prada I, Pereira Bueno S, Butron M, Colina F.
Gastroenterol Hepatol. 1998;21(1):10-2.
Jaundice
Biopsy Homo sapiens Intrahepatic Cholestasis Liver Liver Cirrhosis Male Middle Aged Portal Hypertension
1
(4.0%)
7483697
[Idiopathic ductopenia of adulthood: favorable effect of ursodeoxycholic acid therapy].
Hartmann H, Grone HJ.
Z Gastroenterol. 1993;31 Suppl 2:131-3.
Cholestasis
Biopsy Cholangiography Females Follow-Up Studies Homo sapiens Intrahepatic Cholestasis Liver Liver Function Tests Middle Aged
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 6

HPO ID Term # of case reports
HP:0000821 Hypothyroidism 1
HP:0000952 Jaundice 1
HP:0000989 Pruritus 1
HP:0001394 Cirrhosis 1
HP:0001396 Cholestasis 1
HP:0001409 Portal hypertension 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID