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Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3

Disease ID: disease_node_20258

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DbxrefICD10CM:D84.8, MIM:616910
SubclassofDOID_0090007
Data SourceDOID
SynonymsICF syndrome 3
Doid Labelimmunodeficiency-centromeric instability-facial anomalies syndrome 3
Doid DescriptionAn 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.
Disease Node Iddisease_node_20258
Doid IdDOID_0090010
LabelImmunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3