acute liver failure (Q1192530): Difference between revisions

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Added [ko] description: 질병의 종류, (짧은 설명 도우미)
Removed claim: WikiProjectMed ID (P11143): Acute liver failure, дублирующееся значение / duplicate value
Tag: Manual revert
 
(23 intermediate revisions by 12 users not shown)
label / sllabel / sl
Akutna odpoved jeter
akutna odpoved jeter
label / srlabel / sr
 
Акутна инсуфицијенција јетре
label / azlabel / az
 
Kəskin qaraciyər yetməzliyi
aliases / fr / 0aliases / fr / 0
 
insuffisance hepatique aigue
aliases / fr / 1aliases / fr / 1
 
hépatite fulminante
aliases / fr / 2aliases / fr / 2
 
hepatite fulminante
aliases / fr / 3aliases / fr / 3
 
Hepatitis fulminans
aliases / fr / 4aliases / fr / 4
Insuffisance hépatique aigue
aliases / fr / 5aliases / fr / 5
Insuffisance hepatique aigue
aliases / fr / 6aliases / fr / 6
Hépatite fulminante
aliases / fr / 7aliases / fr / 7
Hepatite fulminante
aliases / fr / 8aliases / fr / 8
Hépatite fulminans
description / frdescription / fr
 
maladie
Property / MeSH descriptor ID: D017114 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / MeSH descriptor ID: D017114 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / subclass of: rare parenchymal liver disease / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / subclass of: rare parenchymal liver disease / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / ICD-10-CM: K72.0 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / ICD-10-CM: K72.0 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / Mondo ID
 
Property / Mondo ID: MONDO:0019542 / rank
Normal rank
 
Property / Mondo ID: MONDO:0019542 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / NCI Thesaurus ID: C84396 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / NCI Thesaurus ID: C84396 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / UMLS CUI: C0162557 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / UMLS CUI: C0162557 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / Orphanet ID: 90062 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0019542
Property / Orphanet ID: 90062 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0019542
 
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / Encyclopedia of China (Third Edition) ID
 
Property / Encyclopedia of China (Third Edition) ID: 630453 / rank
 
Normal rank
Property / WikiProjectMed ID
 
Property / WikiProjectMed ID: Acute liver failure / rank
 
Normal rank
Property / Mondo ID
 
Property / Mondo ID: MONDO_0019542 / rank
 
Normal rank
Property / Medical Dictionary for Regulatory Activities ID
 
Property / Medical Dictionary for Regulatory Activities ID: 10019663 / rank
 
Normal rank
Property / Medical Dictionary for Regulatory Activities ID: 10019663 / reference
 
links / srwiki / namelinks / srwiki / name
 
links / azwiki / namelinks / azwiki / name
 

Latest revision as of 07:40, 15 June 2024

rapid deterioration of liver function causing encephalopathy and coagulopathy
  • acute fulminant hepatic failure
  • Acute hepatic failure
  • Fulminant hepatic failure
  • liver failure, acute
Language Label Description Also known as
English
acute liver failure
rapid deterioration of liver function causing encephalopathy and coagulopathy
  • acute fulminant hepatic failure
  • Acute hepatic failure
  • Fulminant hepatic failure
  • liver failure, acute

Statements

Identifiers

0 references
DB91.1
Other acute or subacute hepatic failure
0 references
0 references