Fanconi anemia

This code represents Fanconi anemia, a rare, inherited genetic disorder characterized by bone marrow failure, physical abnormalities, and an increased risk of cancer. It results from defects in DNA repair proteins, leading to chromosomal instability.

Assign this code for patients diagnosed with Fanconi anemia based on genetic testing, clinical presentation, and bone marrow biopsy findings. Documentation should clearly indicate the diagnosis of Fanconi anemia, distinguishing it from other anemias or syndromes.

• Do not confuse with Fanconi syndrome (E72.0-), which is a kidney disorder and is an Excludes1 note.
• Code any associated physical abnormalities (e.g., skeletal, renal) or malignancies separately.
• Ensure documentation specifies "Fanconi anemia" and not just "anemia" to support this specific code.