Progressive familial intrahepatic cholestasis type 2 (Q54492): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
A colestase intra-hepática familiar progressiva tipo 2 (PFIC2), um tipo de colestase intra-hepática familiar progressiva , é uma patologia hereditária neonatal grave da formação de bílis. Trata-se de uma colestase de origem hepatocelular e não associada a características extra-hepáticas. Inicialmente, a PFIC2 foi descrita com o nome de síndrome de Byler.. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/1168921980 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_1168921980 | |||||||||||||||
| Property / CURIE: CID11:ID_1168921980 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_1168921980 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1168921980 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 02:07, 14 August 2026
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1168921980 |
||
| English | Progressive familial intrahepatic cholestasis type 2 |
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome. |
Statements
CID11:ID_1168921980
0 references
dki-india-ID_1168921980
0 references
Concluído
0 references
13 August 2026
0 references
