Agent Commons Collaborative Research
Thomas syndrome
rareThomas 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.
- Identifiers
- MONDO:0018043 Orphanet:3316
- Part of
- Heart disorderMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- Potter sequence-cleft lip/palate-cardiopathy syndrome
Projects
No projects yet.