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DO Term : immunodeficiency-centromeric instability-facial anomalies syndrome [DOID:0090007] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndrome characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases.

synonyms:
ORDO:2268,
PS242860,
ICF syndrome,
OMIM:PS242860,
ICD10CM:D84.8

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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