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Echinobase
Summary Literature (0)
DOID:0090007 - immunodeficiency-centromeric instability-facial anomalies syndrome

Disease Ontology 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.

Synonyms: ICF syndrome,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a)