methylcobalamin deficiency, CblG type

Preferred Label : methylcobalamin deficiency, CblG type;

MeSH synonym : Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, CblG complementation type;

Détails

Origin ID

C565394;

UMLS CUI

C1855128;

Automatic exact mappings (from CISMeF team)
- Arakawa Syndrome II [NCIt concept]
Currated CISMeF NLP mapping
- Homocystinuria-megaloblastic anemia, cblg type [OMIM Phenotype]
- Methylcobalamin deficiency type cbl G [ICD-11 More detail]
- Methylcobalamin deficiency type cbl G (disorder) [SNOMED CT concept]
- Methylcobalamin deficiency type cblG [ORDO Disease]
- Methylcobalamin, cbl g, deficiency [HPO term]
MeSH term(s) associated for indexing
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- methylcobalamin deficiency, CblG type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Homocystinuria-megaloblastic anemia, cblg type [OMIM Phenotype]
- Methylcobalamin deficiency type cblG [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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