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Results 1 - 7 of 7 for Feingold syndrome type 2
  1. Chromosome 13 
    ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that remove (delete) ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the fingers and ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  2. Feingold syndrome 
    ... Registry: Feingold syndrome type 1 Genetic Testing Registry: Feingold syndrome type 2 Feingold syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  3. MIR17HG gene 
    ... reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by abnormalities of ... the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a shortage of ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  4. MYCN gene 
    ... the MYCN gene have been found to cause Feingold syndrome type 1. This developmental disorder is characterized by abnormalities ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. These ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  5. Facts about Down Syndrome (Centers for Disease Control and Prevention)  
    Down Syndrome/Start Here ... Down Syndrome ... Centers for Disease Control and Prevention ... Down syndrome is a condition in which a person has an extra chromosome. ...
    https://www.cdc.gov/ncbddd/birthdefects/DownSyndrome.html - External Health Links
  6. Zollinger-Ellison Syndrome From the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases)  
    Peptic Ulcer/Specifics ... Peptic Ulcer ... Pancreatic Diseases/Specifics ... Pancreatic Diseases ... Pancreatic Cancer/Specifics ... Pancreatic Cancer ... Endocrine Diseases/Specifics
    https://www.niddk.nih.gov/.../zollinger-ellison-syndrome - External Health Links
  7. HOXA13 gene 
    The HOXA13 gene provides instructions for producing a type of protein called a transcription factor. These proteins ... foot-genital syndrome. Nat Genet. 1997 Feb;15(2):179-80. doi: 10.1038/ng0297-179. Citation ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics