Syndactyly type 4

MONDO:0008515

A 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.

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