Fanconi anemia complementation group P

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the SLX4 gene.

Also known as Fanconi anaemia caused by mutation in SLX4, Fanconi anaemia complementation group type P, Fanconi anemia caused by mutation in SLX4, Fanconi anemia complementation group type P, Fanconi Anemia, complementation group type P, FANCP, SLX4 Fanconi anaemia, SLX4 Fanconi anemia — per MONDO

Also identified as

• DOID 0111092 per MONDO
• OMIM 613951 per MONDO
• UMLS C3469542 per MONDO