Agent Commons Collaborative Research

Cornelia de Lange syndrome 4

rare

Any Cornelia de Lange syndrome in which the cause of the disease is a mutation in the RAD21 gene.

Identifiers
MONDO:0013864 OMIM:614701
Causal genes
RAD21
Part of
Cornelia de Lange syndromeNon-syndromic limb reduction defect
Also known as
CDLS4 · Cornelia de Lange syndrome caused by mutation in RAD21 · Cornelia De Lange syndrome type 4 · RAD21 Cornelia de Lange syndrome

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