SAMD9L-Related Predisposition to Myelodysplastic Syndrome

**Semantic type:** Finding

**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.

**Synonyms:** - SAMD9L-Related Myelodysplastic Syndrome Predisposition