Hexokinase deficiency (Q5749049): Difference between revisions

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‎Created claim: ICD-10 ID (P494), D55.2
 
(30 intermediate revisions by 12 users not shown)
label / frlabel / fr
 
déficit en hexokinase
aliases / en / 0aliases / en / 0
 
Nonspherocytic hemolytic anemia due to hexokinase deficiency
aliases / en / 1aliases / en / 1
 
Hexokinase deficiency hemolytic anemia
aliases / en / 2aliases / en / 2
 
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
description / endescription / en
 
medical condition
description / ukdescription / uk
 
медичний стан
Property / P107 (Deleted Property)
term Property P107 not found, cannot determine the data type to use.
 
Property / P107 (Deleted Property): term Property P107 not found, cannot determine the data type to use. / rank
Normal rank
 
Property / P107 (Deleted Property): term Property P107 not found, cannot determine the data type to use. / reference
 
Property / OMIM ID: 235700 / qualifier
 
Property / OMIM ID: 235700 / 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_0009340
Property / ICD-10 ID: D55.2 / reference
 
Property / health specialty
 
Property / health specialty: hematology / rank
 
Normal rank
Property / MeSH descriptor ID
 
Property / MeSH descriptor ID: C562995 / rank
 
Normal rank
Property / MeSH descriptor ID: C562995 / qualifier
 
Property / MeSH descriptor ID: C562995 / 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_0009340
Property / ICD-10-CM
 
Property / ICD-10-CM: D55.2 / rank
 
Normal rank
Property / ICD-10-CM: D55.2 / 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_0009340
Property / GARD rare disease ID
 
Property / GARD rare disease ID: 3672 / rank
 
Normal rank
Property / GARD rare disease ID: 3672 / 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_0009340
Property / UMLS CUI
 
Property / UMLS CUI: C3150343 / rank
 
Normal rank
Property / UMLS CUI: C3150343 / qualifier
 
Property / UMLS CUI: C3150343 / 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_0009340
Property / UMLS CUI
 
Property / UMLS CUI: C0472792 / rank
 
Normal rank
Property / UMLS CUI: C0472792 / qualifier
 
Property / UMLS CUI: C0472792 / 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_0009340
Property / UMLS CUI
 
Property / UMLS CUI: C3502059 / rank
 
Normal rank
Property / UMLS CUI: C3502059 / reference
 
based on heuristic: inferred by common MeSH mappings on source and on Wikidata
stated in: UMLS 2023
retrieved: 25 May 2023
Timestamp+2023-05-25T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / UMLS CUI
 
Property / UMLS CUI: C5681378 / rank
 
Normal rank
Property / UMLS CUI: C5681378 / reference
 
based on heuristic: inferred by common Orphanet mappings on source and on Wikidata
stated in: UMLS 2023
retrieved: 16 June 2023
Timestamp+2023-06-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Orphanet ID
 
Property / Orphanet ID: 90031 / rank
 
Normal rank
Property / Orphanet ID: 90031 / qualifier
 
Property / Orphanet ID: 90031 / 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_0009340
Property / subclass of
 
Property / subclass of: hemolytic anemia due to a disorder of glycolytic enzymes / rank
 
Normal rank
Property / subclass of: hemolytic anemia due to a disorder of glycolytic enzymes / 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_0009340
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_90031 / rank
 
Normal rank
Property / Microsoft Academic ID
 
Property / Microsoft Academic ID: 2779994328 / rank
 
Normal rank
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / genetic association
 
Property / genetic association: HK1 / rank
 
Normal rank
Property / genetic association: HK1 / reference
 
Property / UniProt disease ID
 
Property / UniProt disease ID: DI-01739 / rank
 
Normal rank
Property / Mondo ID
 
Property / Mondo ID: MONDO_0009340 / rank
 
Normal rank

Latest revision as of 20:02, 25 February 2024

medical condition
  • Nonspherocytic hemolytic anemia due to hexokinase deficiency
  • Hexokinase deficiency hemolytic anemia
  • HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
Language Label Description Also known as
English
Hexokinase deficiency
medical condition
  • Nonspherocytic hemolytic anemia due to hexokinase deficiency
  • Hexokinase deficiency hemolytic anemia
  • HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY

Statements

Identifiers

Mondo ID
MONDO_0009340
0 references
 
                  Retrieved from "https://www.wikidata.org/w/index.php?title=Q5749049&oldid=2087146406"