immunodeficiency-centromeric instability-facial anomalies syndrome 3

Summary

DOID:0090010 - immunodeficiency-centromeric instability-facial anomalies syndrome 3

Disease Ontology Definition:An immunodeficiency-centromeric instability-facial anomalies syndrome characterized by autosomal recessive inheritance, recurrent infections in childhood and variable dysmorphic facial features that has_material_basis_in homozygous mutation in the CDCA7 gene on chromosome 2q31.

Synonyms: ICF syndrome 3

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cdca7

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014828 - immunodeficiency-centromeric instability-facial anomalies syndrome 3

MONDO:0014828 - immunodeficiency-centromeric instability-facial anomalies syndrome 3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): immunodeficiency-centromeric instability-facial anomalies syndrome (is_a)