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Thomas syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description Thomas syndrome is characterised by renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive.
Mondo Term and Equivalent IDs
MONDO:0018043:  Thomas syndrome
GARD:0005175: 
MESH:C536514: 
Orphanet:3316: 
SCTID:716740009: 
UMLS:C2931225: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found