Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, CblE complementation type

Preferred Label : Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, CblE complementation type;

UMLS semantic type : T047 - Disease or Syndrome;

Détails

Origin ID

M0565810;

UMLS CUI

C1856057;

Automatic exact mappings (from CISMeF team)
- Homocystinuria-megaloblastic anemia, cble type [OMIM Phenotype]
Related record
- Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, CblE complementation type [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Homocystinuria-Megaloblastic Anemia, cblE Complementation Type [NCIt concept]
- Homocystinuria-megaloblastic anemia, cble type [OMIM Phenotype]
- Methylcobalamin deficiency type cbl E [ICD-11 More detail]
- Methylcobalamin deficiency type cblE [ORDO Disease]

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

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