|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Floating-Harbor syndrome is a genetic developmental disorder characterized by facial dysmorphism, short stature with delayed bone age, and expressive language delay. (Orphanet Rare Disease Ontology, Orphanet_2044)|
|Downloads & Tools|
1 genes associated with the Floating-Harbor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|SRCAP||Snf2-related CREBBP activator protein|