A group of genes that works together to produce a person’s physical characteristics. Prior to the identification of the genes and genetic mutations that cause Fanconi anemia (FA), patients with the disease were classified into sub-categories known as complementation groups based on the patient’s cellular features. These complementation groups correspond to the various FA genes (e.g., individuals who belong to complementation group A have mutations in the FANCA gene, whereas individuals who belong to complementation group B have mutations in the FANCB gene).
« Back to Glossary IndexNews
Related News
Sep 27th, 2024
Katherine (middle) with 2023's recipient Ana Tabar (left) and FCF CEO Isis Sroka (right) The De Los Santos family first experienced the complexities of Fanconi anemia as they endured the devastating loss of their daughter, Gracie, who passed away from...
Feb 25th, 2025
By Kelly McKenna My name is Kelly McKenna, and I’m a single mom to two amazing kids. One of them is an eight-year-old boy who has Fanconi anemia (FA). Logan’s medical journey started during my pregnancy at the 20-week anatomy...
Dec 11th, 2024
This virtual meeting is an opportunity for individuals diagnosed with Fanconi Anemia Neurological Syndrome (FANS) and their families to gather, share experiences, and find mutual support for navigating FANS. Registration is required and participants must speak English as interpretation is...