Intrahepatic cholestasis
Symptom Information:
Symptom ID: | HPO:0001406 | ||
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 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: |
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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) |