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C157747Level 8

TSC2 Monoallelic Inactivation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the TSC2 gene.

**Synonyms:** - Monoallelic TSC2 Gene Inactivation - Monoallelic Tuberin Gene Inactivation - Monoallelic Tuberous Sclerosis 2 Gene Inactivation - TSC2 LOH - TSC2 Loss of Heterozygosity - TSC2 Monoallelic Gene Inactivation

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