Search Ontology:
Human Disease
Fanconi anemia complementation group W
- Term ID
- DOID:0060978
- Synonyms
-
- Definition
- A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the RFWD3 gene on chromosome 16q23. https://pubmed.ncbi.nlm.nih.gov/28691929/
- References
- Ontology
- Human Disease ( DOID:0060978 )
- is a type of
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Zebrafish Models