Ritscher-Schinzel syndrome 2

MONDO:0010499

Any Ritscher-Schinzel syndrome in which the cause of the disease is a mutation in the CCDC22 gene.

Also known as: CCDC22 Ritscher-Schinzel syndrome, RTSC2, Ritscher-Schinzel syndrome 2, Ritscher-Schinzel syndrome 2, X-linked recessive, Ritscher-Schinzel syndrome caused by mutation in CCDC22, Ritscher-Schinzel syndrome type 2

1 clinical trial for this condition and its sub-types, 0 tagged with Ritscher-Schinzel syndrome 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Ritscher-Schinzel syndrome (0)

Including sub-types (1) Tagged with Ritscher-Schinzel syndrome 2 (0)

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