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Synpolydactyly type 1
rareAny non-syndromic synpolydactyly in which the cause of the disease is a mutation in the HOXD13 gene.
- Identifiers
- MONDO:0008513 OMIM:186000Orphanet:295195
- Causal genes
- HOXD13
- Also known as
- HOXD13 non-syndromic synpolydactyly · non-syndromic synpolydactyly caused by mutation in HOXD13 · SD2, Vordingborg type · SD2a · SPD, Vordingborg type
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