Acrocephalosyndactylia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A synostosis that results_in craniosynostosis and syndactyly. (Human Disease Ontology, DOID_12960)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000168
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Genes

2 genes/proteins associated with the disease Acrocephalosyndactylia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TWIST1 twist family bHLH transcription factor 1 2.88009
FGFR2 fibroblast growth factor receptor 2 2.88009