Cerebrooculofacioskeletal syndrome 2

MONDO:0012553

Any COFS syndrome in which the cause of the disease is a mutation in the ERCC2 gene.

Also known as: COFS syndrome caused by mutation in ERCC2, COFS2, ERCC2 COFS syndrome, cerebrooculofacioskeletal syndrome 2, cerebrooculofacioskeletal syndrome type 2

3 clinical trials for this condition and its sub-types, 0 tagged with Cerebrooculofacioskeletal syndrome 2 itself.

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↑ COFS syndrome (1)

Including sub-types (3) Tagged with Cerebrooculofacioskeletal syndrome 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.