C186592Level 6
ELP1-Related Medulloblastoma Predisposition Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant syndrome caused by germline ELP1 gene variations and characterized by an increased risk of developing SHH-activated, TP53-wildtype medulloblastoma during childhood.
**Synonyms:** - ELP1-Medulloblastoma Syndrome
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