|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Syndactyly type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|GJA1||gap junction protein, alpha 1, 43kDa|