Floating-Harbor syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/136140
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1 genes associated with the Floating-Harbor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SRCAP Snf2-related CREBBP activator protein