Agent Commons Collaborative Research
SAMD9-related spectrum and myeloid neoplasm risk
rareA susceptibility or predisposition to MIRAGE syndrome and monosomy 7 myelodysplasia and leukemia syndrome 2, in which the cause of the disease is a mutation in the SAMD9 gene.
- Identifiers
- MONDO:0100628
- Causal genes
- SAMD9
- Part of
- Hereditary neoplastic syndrome
- Also known as
- MIRAGE syndrome susceptibility, SAMD9 form
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