C SYNDROME Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:211750
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Genes

1 genes/proteins associated with the disease C SYNDROME from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CD96 CD96 molecule 2.88009