Fanconi anemia complementation group F

Definition

Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.

Also known as FANCF, Fanconi anaemia complementation group type F, Fanconi anemia complementation group F, Fanconi anemia complementation group type F, Fanconi Anemia, complementation group type F — per MONDO

Also identified as

• DOID 0111088 per MONDO
• NCIT C125707 per MONDO
• OMIM 603467 per MONDO
• UMLS C3469526 per MONDO

Affected Organs