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Disease Ontology Browser
Kenny-Caffey syndrome type 2 (DOID:0080723)
Alliance: disease page
Alt IDs: OMIM:127000, ORDO:93325
Definition: A Kenny-Caffey syndrome that has_material_basis_in heterozygous mutation in the FAM111A gene on chromosome 11q12.


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
09/13/2022
MGI 6.21
The Jackson Laboratory