Thomas syndrome

MONDO:0018043

Thomas syndrome is characterized by renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive.

Also known as: Potter sequence-cleft lip/palate-cardiopathy syndrome

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

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Heart disorder (6782) ↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163)

Including sub-types (0) Tagged with Thomas syndrome (0)

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