Disorders of fructose metabolism

Preferred Label : Disorders of fructose metabolism;

ICD-10 exclusion note : muscle phosphofructokinase deficiency (E74.09);

Diag associé à un acte (%) : 50.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E741;

UMLS CUI

C0342744;

Automatic exact mappings (from CISMeF team)
- Hereditary Fructose Intolerance [NCIt concept]
- fructose intolerance [MeSH Descriptor]
- fructose intolerance [MeSH concept]
CISMeF manual mappings
- Essential fructosuria [ORDO Disease]
- Fructose-1,6-bisphosphatase deficiency [ORDO Disease]
Currated CISMeF NLP mapping
- Disorder of fructose metabolism [ORDO Disease]
- Disorders of fructose metabolism [ICD-11 Subcategory]
- Fructose metabolism disorder (disorder) [SNOMED CT concept]
- Fructose-1,6-Diphosphatase deficiency [MeSH concept]
- Fructosuria [MeSH concept]
- Fructosuria, essential [OMIM Phenotype]
- Impairment of fructose metabolism [HPO term]
- disorders of fructose metabolism [Error of metabolism category]
- essential benign fructosuria [SNOMED Notion]
- fructose disorder, nos [SNOMED Notion]
- fructose metabolism disorder [Disease (Nov.)]
- fructose-1,6-diphosphatase deficiency [MeSH Descriptor]
- fructose-biphosphatase deficiency [SNOMED Notion]
- fructosuria [MeSH Supplementary Concept]
Orphanet concepts
- Disorder of fructose metabolism [ORDO Disease]
- Essential fructosuria [ORDO Disease]
- Fructose-1,6-bisphosphatase deficiency [ORDO Disease]
- Hereditary fructose intolerance [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder of fructose metabolism [ORDO Disease]
- Fructose metabolism disorder (disorder) [SNOMED CT concept]
- fructose disorder, nos [SNOMED Notion]
- fructose metabolism disorder [Disease (Nov.)]
Validated automatic mappings to BTNT
- Hereditary fructose intolerance [ICD-11 Sub-sub category]
- essential fructosuria [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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