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immunodeficiency-centromeric instability-facial anomalies syndrome (DOID:0090007)
Alliance: disease page
Synonyms: ICF syndrome
Alt IDs: ICD10CM:D84.8, OMIM:PS242860, ORDO:2268
Definition: A syndrome characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases.

Disease References using Mouse Models (2)

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
MGI 6.22
The Jackson Laboratory