Syndactyly type 3 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Syndactyly type 3 (SD3) is a rare congenital distal limb malformation characterized by complete and bilateral syndactyly between the 4th and 5th fingers. (Orphanet Rare Disease Ontology, Orphanet_93404)
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1 genes associated with the Syndactyly type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa