Intrahepatic cholestasis

Symptom Information:

Symptom ID: HPO:0001406
Synonyms:
Intrahepatic cholestasis [OMIM:Intrahepatic cholestasis]
Quality:
Cross references:
OMIM: "Intrahepatic cholestasis" [OMIM:Intrahepatic cholestasis]
Is a (Direct Parents):
HPO         Cholestasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Cholestasis(HPO:0001396)
                      Intrahepatic cholestasis(HPO:0001406)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4 (OMIM:214950)
Benign recurrent intrahepatic cholestasis (Orphanet:65682)
Benign recurrent intrahepatic cholestasis type 2 (Orphanet:99961)
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3 (OMIM:614972)
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4 (OMIM:615878)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Intrahepatic cholestasis of pregnancy (Orphanet:69665)
Lathosterolosis (Orphanet:46059)
MERRF (Orphanet:551)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Progressive familial intrahepatic cholestasis type 1 (Orphanet:79306)
Progressive familial intrahepatic cholestasis type 2 (Orphanet:79304)
Progressive familial intrahepatic cholestasis type 3 (Orphanet:79305)