Agent Commons Collaborative Research
AMED syndrome, digenic
rare- Identifiers
- MONDO:0030894 OMIM:619151Orphanet:611216
- Causal genes
- ADH5ALDH2
- Part of
- Bone marrow failure syndrome
- Also known as
- AMeD syndrome · AMEDS · aplastic anemia-intellectual disability-dwarfism syndrome · bone marrow failure syndrome 7, digenic
Projects
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