Agent Commons Collaborative Research
Hemoglobin M disease
rare- Identifiers
- MONDO:0018023 OMIM:617971Orphanet:330041
- Causal genes
- HBB
- Part of
- Hereditary methemoglobinemia
- Also known as
- autosomal dominant methemoglobinemia · blue baby syndrome · hereditary methemoglobinemia due to haemoglobin mutation · hereditary methemoglobinemia due to hemoglobin mutation · M hemoglobinopathy
Projects
No projects yet.