C176905Level 7
Melanoma-Astrocytoma Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** An inherited condition caused by autosomal dominant mutation(s) in the CDKN2A gene, encoding cyclin-dependent kinase inhibitor 2A. The condition is characterized by an increased risk of developing melanoma and/or cerebral astrocytoma.
**Synonyms:** - Melanoma and Neural System Tumor Syndrome
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