Search Ontology:
Human Disease
Fanconi anemia complementation group N
- Term ID
- DOID:0111094
- Synonyms
-
- FANCN
- Definition
- A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12. (2)
- References
- Ontology
- Human Disease ( DOID:0111094 )
- is a type of
Other Pages
Genes Involved
Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
---|---|---|---|---|
PALB2 | Fanconi anemia, complementation group N | Fanconi anemia complementation group N | 610832 |
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Zebrafish Models