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synpolydactyly

term may be used synonymously with synpolydactyly type II Genetics: 1) chromosomal translocation involving RASSF8 t(12;22)(p11.2;q13.3) with FBLN1 is found in a complex type of synpolydactyly 2) autosomal dominant trait with reduced penetrance associated with defects in HOXD13 Clinical manifestations: - associated polydactyly & syndactyly - limb malformation that shows a characteristic manifestation in both hands & feet

General

syndactyly

Database Correlations

OMIM 186000

References

  1. http://medical-dictionary.com/
  2. OMIM :accession 186000