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C184315Level 6

Monoallelic PALB2 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 PALB2 gene.

**Synonyms:** - Monoallelic FANCN Gene Inactivation - Monoallelic Fanconi Anemia, Complementation Group N Gene Inactivation - Monoallelic Inactivating PALB2 Gene Mutation - Monoallelic Inactivating PALB2 Mutation - Monoallelic PALB2 Inactivating Gene Mutation - Monoallelic PALB2 Inactivating Mutation - Monoallelic PALB2 Inactivation - Monoallelic PALB2 Loss of Function - Monoallelic PALB2 Loss of Function Gene Mutation - Monoallelic PALB2 Loss of Function Mutation - Monoallelic PNCA3 Gene Inactivation - Monoallelic Partner and Localizer of BRCA2 Gene Inactivation - PALB2 Gene LOH - PALB2 Homozygous Loss - PALB2 Loss of Heterozygosity

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