C syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/211750
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Genes

1 genes associated with the C syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CD96 CD96 molecule