Seckel syndrome 1

MONDO:0008869

Any Seckel syndrome in which the cause of the disease is a mutation in the ATR gene.

Also known as: ATR Seckel syndrome, SCKL1, Seckel syndrome 1, Seckel syndrome 3, Seckel syndrome caused by mutation in ATR, Seckel syndrome type 1, Bird-headed dwarfism, Sckl

0 clinical trials for this condition and its sub-types, 0 tagged with Seckel syndrome 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Seckel syndrome (1)

Including sub-types (0) Tagged with Seckel syndrome 1 (0)

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