World Of Taxonomy
C222069Level 5

TRIP13 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the TRIP13 gene.

**Synonyms:** - 16E1BP Gene Mutation - PCH2 Gene Mutation - Thyroid Hormone Receptor Interactor 13 Gene Mutation

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C222069 - TRIP13 Gene Mutation - NCI Thesaurus - World Of Taxonomy | World Of Taxonomy