Syndactyly type 3 (SD3) is a rare congenital distal limb malformation characterized by complete and bilateral syndactyly between the 4th and 5th fingers.
Matched Phenotype
Gene
Mutation
MeSH
Rank
(Similarity) |
PMID
(PMCID) |
Phenotype(s) retrieved from Orphanet
Total: 3
| HPO ID |
Term |
Frequency |
| HP:0006101 |
Finger syndactyly |
Very frequent (99-80%) |
| HP:0100490 |
Camptodactyly of finger |
Frequent (79-30%) |
| HP:0001831 |
Short toe |
Occasional (29-5%) |
Phenotype(s) retrieved from case reports
Total: 0
| HPO ID |
Term |
# of case reports |
Causative gene(s) retrieved from Orphanet
Total: 1
| Gene Symbol |
Gene Name |
Entrez Gene ID |
| GJA1 |
gap junction protein alpha 1 |
2697 |
