hnsha due to aldolase deficiency - CISMeF

" /> hnsha due to aldolase deficiency - CISMeF

CISMeF

chu

Hnsha due to aldolase deficiencySNOMED Notion

Preferred Label : hnsha due to aldolase deficiency;

Details

Origin ID

DC-17170;

UMLS CUI

C0272066;

Currated CISMeF NLP mapping
- Glycogen storage disease XII [OMIM Phenotype]
- Glycogen storage disease due to aldolase A deficiency [ORDO Disease]
- Glycogen storage disease due to aldolase A deficiency [ICD-11 More detail]
- Glycogen storage disease due to aldolase A deficiency (disorder) [SNOMED CT concept]
- Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) [Inactive SNOMED CT concept]
- glycogen storage disease XII [MeSH Supplementary Concept]
- glycogen storage disease XII [MeSH concept]
ICD-10 exact mapping(s)
- Anaemia due to disorders of glycolytic enzymes [ICD-10 Sub-category (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED CT concept
- Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) [Inactive SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glycogen storage disease XII [OMIM Phenotype]
- Glycogen storage disease due to aldolase A deficiency [ORDO Disease]
- Glycogen storage disease due to aldolase A deficiency [ICD-11 More detail]
- Glycogen storage disease due to aldolase A deficiency (disorder) [SNOMED CT concept]
- Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) [Inactive SNOMED CT concept]
- glycogen storage disease XII [MeSH Supplementary Concept]
- glycogen storage disease XII [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
20/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.