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Methylcobalamin deficiency type cblDv1

MedGen UID:: 1826168
•Concept ID:: C5679956
•: Disease or Syndrome

Synonyms:	Functional methionine synthase deficiency type cblDv1; functional methionine synthase deficiency type cblDv1; methylcobalamin deficiency type cblDv1

Monarch Initiative:	MONDO:0017683
Orphanet:	ORPHA308380

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MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVMethylcobalamin deficiency type cblDv1

Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder
- Homocystinuria without methylmalonic aciduria
  - Methylcobalamin deficiency type cblDv1

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Methylcobalamin deficiency type cblDv1
Methylcobalamin deficiency type cblDv1

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