lactate dehydrogenase deficiency type A

Preferred Label : lactate dehydrogenase deficiency type A;

MeSH synonym : GSD11; lactate dehydrogenase A deficiency;

Origin ID

C538133;

UMLS CUI

C2931743;

Currated CISMeF NLP mapping
- Glycogen storage disease XI [OMIM Phenotype]
- Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency [ORDO Disease]
- Glycogen storage disease due to lactate dehydrogenase deficiency [ORDO Disease]
- Lactate dehydrogenase deficiency (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- L-Lactate dehydrogenase [MeSH Descriptor]
- glycogen storage disease [MeSH Descriptor]
Record concept(s)
- Lactate dehydrogenase deficiency type A [MeSH concept]
See also inter- (CISMeF)
- Glycogen storage disease due to lactate dehydrogenase deficiency [ORDO Disease]
- glycogen storage disease type 11 [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glycogen storage disease XI [OMIM Phenotype]
- Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency [ORDO Disease]
- glycogen storage disease type 11 [Disease (Nov.)]
Validated automatic mappings to NTBT
- Lactate dehydrogenase deficiency [ICD-11 Sub-sub category]