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Results 1 - 6 of 6 for Feingold syndrome type 1
  1. Feingold syndrome 
    ... that can vary among affected individuals.Individuals with Feingold syndrome type 1 or type 2 have characteristic abnormalities of their ... stature, or kidney or heart abnormalities.People with Feingold syndrome type 1 are frequently born with a blockage in part ...
    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 abnormalities of ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. These genetic ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  3. Chromosome 13 
    ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that remove ( ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the fingers ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  4. MIR17HG gene 
    ... reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by abnormalities ... the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a shortage ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  5. 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):197-202. doi: 10.1086/302961. Epub 2000 ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics
  6. ORC1 gene 
    ... HSORC1 ORC1_HUMAN ORC1L origin recognition complex, subunit 1 origin recognition complex, subunit 1 homolog PARC1 replication control protein 1 Tests of ...
    https://medlineplus.gov/genetics/gene/orc1 - Genetics