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Syndactyly type 4

rare

A very rare congenital distal limb malformation characterized by complete bilateral syndactyly (involving all digits 1 to 5).

Identifiers
MONDO:0008515 OMIM:186200Orphanet:93405
Causal genes
LMBR1
Part of
Non-syndromic syndactylyPolydactyly-syndactyly-triphalangism
Also known as
LMBR1 non-syndromic syndactyly · non-syndromic syndactyly caused by mutation in LMBR1 · polysyndactyly type Haas · polysyndactyly, Haas type · SDTY4

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