Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency

Preferred Label : Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency;

Inclusion CIM-10 : G6PD deficiency anemia; Favism;

Diag associé à un acte (%) : 61.4;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D550;

UMLS CUI

C0237987;

Currated CISMeF NLP mapping
- Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency [ICD-10 Sub-category (who)]
- Deficiency of glucose-6-phosphate dehydrogenase (disorder) [SNOMED CT concept]
- Favism [NCIt concept]
- Favism [MedDRA LLT]
- Favism (disorder) [SNOMED CT concept]
- G-6 PD deficiency [MedDRA LLT]
- G6PD deficiency [MedDRA LLT]
- Glucose-6-Phosphate Dehydrogenase Deficiency [NCIt concept]
- Glucose-6-Phosphate dehydrogenase [LOINC component]
- Glucose-6-phosphate dehydrogenase [OMIM gene]
- Glucose-6-phosphate dehydrogenase deficiency [MedDRA Preferred Term]
- Glucose-6-phosphate dehydrogenase deficiency anemia (disorder) [SNOMED CT concept]
- Glucose-6-phosphate-dehydrogenase deficiency [ORDO Disease]
- Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency [ICD-11 Sub-sub category]
- favism [MeSH concept]
- favism [DO Concept]
- glucose-6-phosphate dehydrogenase deficiency anemia, nos [SNOMED Notion]
- glucosephosphate dehydrogenase deficiency [MeSH concept]
- vicia faba poisoning [SNOMED Notion]
DO Cross reference
- favism [DO Concept]
Orphanet concepts
- Class I glucose-6-phosphate dehydrogenase deficiency [ORDO Disease]
- Glucose-6-phosphate-dehydrogenase deficiency [ORDO Disease]
- Rare constitutional hemolytic anemia due to an enzyme disorder [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ANAEMIA HAEMOLYTIC G6PD [WHO-ART Preferred Term]
- Anaemia haemolytic G6PD [MedDRA LLT]
- Anaemia haemolytic G6PD deficiency [MedDRA LLT]
- Anemia hemolytic G6PD [MedDRA LLT]
- Anemia hemolytic G6PD deficiency [MedDRA LLT]
- Glucose-6-phosphate dehydrogenase deficiency anemia (disorder) [SNOMED CT concept]
- Glucose-6-phosphate-dehydrogenase deficiency [ORDO Disease]
- Haemolytic anaemia G6PD deficiency [MedDRA LLT]
- Haemolytic anaemia glucose-6-phos dehydrogenase deficiency [MedDRA LLT]
- Hemolytic anemia G6PD deficiency [MedDRA LLT]
- Hemolytic anemia glucose-6-phos dehydrogenase deficiency [MedDRA LLT]
- glucose-6-phosphate dehydrogenase deficiency anemia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- favism [MeSH Descriptor]
Validated automatic mappings to NTBT
- glucosephosphate dehydrogenase deficiency [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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