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Disease Ontology Browser
Fanconi anemia complementation group P (DOID:0111092)
Alliance: disease page
Synonyms: FANCP
Alt IDs: OMIM:613951
Definition: A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
09/19/2023
MGI 6.22
The Jackson Laboratory