FANCA Biallelic Inactivation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** The presence of mutations in both alleles of the FANCA gene that either lead to loss of expression of the FANCA protein or result in the translation of an inactive FANCA protein.

**Synonyms:** - FA Biallelic Gene Inactivation - FA-H Biallelic Gene Inactivation - FA1 Biallelic Gene Inactivation - FAA Biallelic Gene Inactivation - FACA Biallelic Gene Inactivation - FAH Biallelic Gene Inactivation - FANCA Biallelic Gene Inactivation - FANCH Biallelic Gene Inactivation - Fanconi Anemia Complementation Group A Biallelic Gene Inactivation - Fanconi Anemia, Complementation Group A Biallelic Gene Inactivation - Fanconi Anemia, Complementation Group H Biallelic Gene Inactivation - Fanconi Anemia, Type 1 Biallelic Gene Inactivation