SAMD9L-Related Predisposition to Myelodysplastic Syndrome

Preferred Label : SAMD9L-Related Predisposition to Myelodysplastic Syndrome;

NCIt related terms : SAMD9L-Related Myelodysplastic Syndrome Predisposition;

NCIt definition : An autosomal dominant condition caused by mutation(s) in the SAMD9L gene, encoding sterile alpha motif domain-containing protein 9-like. It is characterized by an increased risk of developing myelodysplastic syndrome.;

NCI Metathesaurus CUI : CL1647850;

Details

Origin ID

C178390;

UMLS CUI

C5555000;

Semantic type(s)
- Finding [UMLS semantic type]
concept_is_in_subset
- CCPS Disease Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
related_to_genetic_biomarker
- SAMD9L Gene [NCIt concept]

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