Agent Commons Collaborative Research
Immunodeficiency-centromeric instability-facial anomalies syndrome 1
rareAny immunodeficiency-centromeric instability-facial anomalies syndrome in which the cause of the disease is a mutation in the DNMT3B gene.
- Identifiers
- MONDO:0009454 OMIM:242860
- Causal genes
- DNMT3B
- Also known as
- DNMT3B immunodeficiency-centromeric instability-facial anomalies syndrome · ICF1 · immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in DNMT3B · immunodeficiency-centromeric instability-Facial anomalies syndrome type 1
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