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Results 1 - 10 of 21 for Syndactyly type 4
  1. GJA1 gene 
    ... GJA1 gene in each cell can cause isolated syndactyly type III, which is characterized by fusion of the ... fingers) and sometimes shortening of the pinky finger. Syndactyly type III is a characteristic feature in oculodentodigital dysplasia ( ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  2. GLI3 gene 
    ... Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet. 2005 Apr;76(4):609-22. doi: 10.1086/429346. Epub 2005 ...
    https://medlineplus.gov/genetics/gene/gli3 - Genetics
  3. Oral-facial-digital syndrome 
    ... The molecular basis of oral-facial-digital syndrome, type 1. Am J Med Genet C Semin Med Genet. 2009 Nov 15;151C(4):318-25. doi: 10.1002/ajmg.c.30224. ...
    https://medlineplus.gov/.../condition/oral-facial-digital-syndrome - Genetics
  4. Feingold syndrome 
    ... inward (clinodactyly), underdeveloped thumbs (thumb hypoplasia), and fusion (syndactyly) of the second and third toes or the fourth and fifth toes.Additional common features of both types of Feingold syndrome include an unusually small head ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  5. Pallister-Hall syndrome 
    ... Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet. 2005 Apr;76(4):609-22. doi: 10.1086/429346. Epub 2005 ...
    https://medlineplus.gov/genetics/condition/pallister-hall-syndrome - Genetics
  6. Greig cephalopolysyndactyly syndrome 
    ... Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet. 2005 Apr;76(4):609-22. doi: 10.1086/429346. Epub 2005 ...
    https://medlineplus.gov/.../greig-cephalopolysyndactyly-syndrome - Genetics
  7. Miller syndrome 
    ... new observation of two cases of acrofacial dysostosis type Genee-Wiedemann in a family--remarks on the mode of inheritance: report on two sibs. Am J Med Genet. 1996 Sep 6;64(4):556-62. doi: 10.1002/(SICI)1096-8628( ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
  8. Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
    https://ccakids.org/.../uploads/2022/01/pfeiffer-guide_2018.pdf - External Health Links
  9. Atelosteogenesis type 3 
    ... may be permanently bent (camptodactyly) or fused together (syndactyly). ... atelosteogenesis type 3 typically have an underdeveloped rib cage that ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-3 - Genetics
  10. Megalencephaly-capillary malformation syndrome 
    ... between two or more fingers or toes (cutaneous syndactyly).Additional features of ... with several types of cancer. Only a small number of individuals ...
    https://medlineplus.gov/...encephaly-capillary-malformation-syndrome - Genetics
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