Other specified diseases of liver

Preferred Label : Other specified diseases of liver;

Diag associé à un acte (%) : 91.1;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2018;

Details

Origin ID

K768;

UMLS CUI

C0348751;

Automatic exact mappings (from CISMeF team)
- Other specified diseases of liver [ICD-11 More detail]
DO Cross reference
- congenital bile acid synthesis defect [DO Concept]
Orphanet concepts
- Bile acid CoA ligase deficiency and defective amidation [ORDO Disease]
- Bile acid synthesis defect with cholestasis and malabsorption [ORDO Disease]
- Congenital bile acid synthesis defect type 1 [ORDO Disease]
- Congenital bile acid synthesis defect type 2 [ORDO Disease]
- Congenital bile acid synthesis defect type 3 [ORDO Disease]
- Congenital bile acid synthesis defect type 4 [ORDO Disease]
- Fibrohistiocytic inflammatory pseudotumor of the liver [ORDO Disease]
- Hyperbiliverdinemia [ORDO Disease]
- Lymphoplasmacytic inflammatory pseudotumor of the liver [ORDO Disease]
- MYO5B-related progressive familial intrahepatic cholestasis [ORDO Disease]
- Nodular regenerative hyperplasia of the liver [ORDO Disease]
- Parenteral nutrition-associated cholestasis [ORDO Disease]
- Portosinusoidal vascular disease [ORDO Disease]
- Progressive familial intrahepatic cholestasis [ORDO Disease]
- Progressive familial intrahepatic cholestasis type 1 [ORDO Disease]
- Progressive familial intrahepatic cholestasis type 2 [ORDO Disease]
- Progressive familial intrahepatic cholestasis type 3 [ORDO Disease]
- Progressive familial intrahepatic cholestasis type 4 [ORDO Disease]
- Progressive familial intrahepatic cholestasis type 5 [ORDO Disease]
- Steroid dehydrogenase deficiency-dental anomalies syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other Specified Diseases of Liver [NCIt concept]
- Other specified disorders of liver [ICD-9 code]
Validated automatic mappings to BTNT
- Nodular regenerative hyperplasia of liver [ICD-11 Subcategory]
- Progressive familial intrahepatic cholestasis [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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