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Results 1 - 10 of 17 for Feingold syndrome
  1. Feingold syndrome 
    Feingold syndrome is a disorder that affects many parts of the body. There are two types of Feingold syndrome, distinguished by their genetic cause; both types ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  2. MYCN gene 
    ... the MYCN gene have been found to cause Feingold syndrome type 1. This developmental disorder is characterized by ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  3. MIR17HG gene 
    ... reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by ... the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  4. Chromosome 13 
    ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  5. Baller-Gerold syndrome 
    ... 1399-0004.1980.tb00126.x. Citation on PubMed Feingold M, Sklower SL, Willner JP, Desnick RH, Cohen MM. Craniosynostosis-radial aplasia: Baller-Gerold syndrome. Am J Dis Child. 1979 Dec;133(12): ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  6. LORICRIN gene 
    ... Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122( ...
    https://medlineplus.gov/genetics/gene/loricrin - Genetics
  7. Vohwinkel syndrome 
    ... Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122( ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
  8. Weill-Marchesani syndrome 
    ... Megarbane A, Samples J, Gorlin RJ, Alswaid A, Feingold J, Le Merrer M, Munnich A, Cormier-Daire V. Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome. Am J Med Genet A. 2003 Dec 1; ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  9. Hand-foot-genital syndrome 
    ... Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Am J Hum Genet. 2000 Jul;67(1): ...
    https://medlineplus.gov/.../condition/hand-foot-genital-syndrome - Genetics
  10. HOXA13 gene 
    ... Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Am J Hum Genet. 2000 Jul;67(1): ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics
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