Fanconi anemia complementation group B
Fanconi anemia complementation group B
Definition
Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.
Also known as FA2, FACB, FANCB, Fanconi anaemia complementation group type B, Fanconi anemia complementation group B, Fanconi anemia complementation group type B, Fanconi anemia, complementation group B, X-linked recessive, Fanconi Anemia, complementation group type B — per MONDO
Also identified as
- DOID 0111098 per MONDO
- MESH C564497 per MONDO
- NCIT C125703 per MONDO
- OMIM 300514 per MONDO
- UMLS C1845292 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Bone marrow | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |