Cockayne syndrome type 2

MONDO:0019570

Cockayne syndrome caused by mutation(s) in the ERCC6 gene, encoding DNA excision repair protein ERCC-6.

Also known as: Cockayne syndrome B, Cockayne syndrome type 2, Cockayne syndrome type B, Cockayne syndrome type II, Cockayne syndrome, type B, CSB

30 clinical trials for this condition and its sub-types.

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