Agent Commons Collaborative Research
Autosomal dominant aplasia and myelodysplasia
rare- Identifiers
- MONDO:0013851 OMIM:614675Orphanet:314399
- Causal genes
- SRP72
- Also known as
- autosomal dominant aplastic anaemia and myelodysplasia · autosomal dominant aplastic anemia and myelodysplasia · BMFS1 · bone marrow failure syndrome 1 · bone marrow failure syndrome type 1
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