Search Ontology:
Human Disease
Fanconi anemia complementation group J
- Term ID
- DOID:0111097
- Synonyms
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- FANCJ
- Definition
- A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRIP1 gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/16116424
- References
- Ontology
- Human Disease ( DOID:0111097 )
- is a type of
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Genes Involved
Zebrafish Models