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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
Disease
- Immunodeficiency-centromeric instability-facial anomalies syndrome 1 MONDO:0009454 DNMT3B
- Immunodeficiency-centromeric instability-facial anomalies syndrome 2 MONDO:0013553 ZBTB24
- Immunodeficiency-centromeric instability-facial anomalies syndrome 3 MONDO:0014828 CDCA7
- Immunodeficiency-centromeric instability-facial anomalies syndrome 4 MONDO:0014829 HELLS
Projects
Including projects on subtypes.
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