|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability. (Orphanet Rare Disease Ontology, Orphanet_1308)|
|Downloads & Tools|
1 genes/proteins associated with the disease C SYNDROME from the curated CTD Gene-Disease Associations dataset.