SAMD9-related spectrum and myeloid neoplasm risk
MONDO:0100628Mondo
Findings
No curated finding names SAMD9-related spectrum and myeloid neoplasm risk yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A 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.
Definition from the Mondo Disease Ontology (MONDO:0100628), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- SAMD9HGNC:1348
- Definitive · ClinGen · Autosomal dominant · 2024
Where it sits
- A kind of
Other names
1 name
Resolves to: SAMD9-related spectrum and myeloid neoplasm risk
- Also called
- MIRAGE syndrome susceptibility, SAMD9 form