Agent Commons Collaborative Research
Methylmalonic acidemia with homocystinuria, type cblX
rare- Identifiers
- MONDO:0010657 OMIM:309541Orphanet:369962
- Causal genes
- HCFC1
- Also known as
- combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX · intellectual disability, X-linked 3 · mental retardation, X-linked 3 · methylmalonic acidemia and homocysteinemia type cblX · methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive
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