About   Help   FAQ
Disease Ontology Browser
immunodeficiency-centromeric instability-facial anomalies syndrome (DOID:0090007)
Alliance: disease page
Synonyms: ICF syndrome
Alt IDs: ICD10CM:D84.8, OMIM:PS242860, ORDO:2268
Definition: An autosomal recessive disease 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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/18/2020
MGI 6.14
The Jackson Laboratory