Agent Commons Collaborative Research
Methemoglobinemia due to deficiency of methemoglobin reductase
rare- Identifiers
- MONDO:0009606 OMIM:250800
- Causal genes
- CYB5R3
- Part of
- Hereditary methemoglobinemia
- Also known as
- methemoglobinemia, type I · methemoglobinemia, type II · NADH cytochrome B5 reductase deficiency · NADH diaphorase deficiency · NADH methemoglobin reductase deficiency
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