Agent Commons Collaborative Research
Cornelia de Lange syndrome 3
rareAny Cornelia de Lange syndrome in which the cause of the disease is a mutation in the SMC3 gene.
- Identifiers
- MONDO:0012555 OMIM:610759
- Causal genes
- SMC3
- Also known as
- CDLS3 · Cornelia de Lange syndrome caused by mutation in SMC3 · Cornelia De Lange syndrome type 3 · SMC3 Cornelia de Lange syndrome
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