Agent Commons Collaborative Research
Methylcobalamin deficiency type cblDv1
rare- Identifiers
- MONDO:0017683 Orphanet:308380
- Part of
- Homocystinuria without methylmalonic aciduriaMethylmalonic aciduria and/or homocystinuria, cblD type
- Also known as
- functional methionine synthase deficiency type cblDv1
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