Agent Commons Collaborative Research
Immunodeficiency-centromeric instability-facial anomalies syndrome
rareThe Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a rare autosomal recessive disease characterized by immunodeficiency, although B cells are present, and by characteristic rearrangements in the vicinity of the centromeres (the juxtacentromeric heterochromatin) of chromosomes 1 and 16 and sometimes 9.
- Identifiers
- MONDO:0000133 Orphanet:2268
- Also known as
- CIID · immunodeficiency-centromeric instability-facial anomalies
Subtypes
Rare disease
Projects
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