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C184320Level 6

Monoallelic RAD51D Gene 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 RAD51D gene.

**Synonyms:** - Monoallelic BROVCA4 Gene Inactivation - Monoallelic Inactivating RAD51D Gene Mutation - Monoallelic Inactivating RAD51D Mutation - Monoallelic R51H3 Gene Inactivation - Monoallelic RAD51 Homolog D Gene Inactivation - Monoallelic RAD51 Paralog D Gene Inactivation - Monoallelic RAD51-Like 3 Gene Inactivation - Monoallelic RAD51D Inactivating Gene Mutation - Monoallelic RAD51D Inactivating Mutation - Monoallelic RAD51D Inactivation - Monoallelic RAD51D Loss of Function - Monoallelic RAD51D Loss of Function Gene Mutation - Monoallelic RAD51D Loss of Function Mutation - Monoallelic RAD51L3 Gene Inactivation - Monoallelic TRAD Gene Inactivation - RAD51D Gene LOH - RAD51D Homozygous Loss - RAD51D Loss of Heterozygosity

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