Syndactyly type 4
MONDO:0008515A very rare congenital distal limb malformation characterized by complete bilateral syndactyly (involving all digits 1 to 5).
Also known as: LMBR1 non-syndromic syndactyly, non-syndromic syndactyly caused by mutation in LMBR1, polysyndactyly, Haas type, Haas type syndactyly, SDTY4, Sd4, polysyndactyly type Haas, syndactyly, type 4
0 clinical trials for this condition and its sub-types, 0 tagged with Syndactyly type 4 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.