Compendium of Cancer Genome Aberrations

GTS5:Juvenile polyposis syndrome (BMPR1A, SMAD4): Difference between revisions

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==Related Terminology==
==Related Terminology==
<span style="color:#0070C0">(''Instructions: This table will have the related terminology from the WHO book <u>autocompleted</u>.)''</span>
 
{| class="wikitable"
{| class="wikitable"
|+
|+
|Acceptable
|Acceptable
|
|Generalized juvenile polyposis; juvenile polyposis coli; juvenile polyposis of infancy; chromosome 10q22.3-q23.2 deletion syndrome; juvenile polyposis of the stomach; familial juvenile polyposis; hamartomatous gastrointestinal polyposis; combined juvenile polyposis / hereditary haemorrhagic telangiectasia (Osler–Weber–Rendu) syndrome
|-
|-
|Not Recommended
|Not Recommended
|
|N/A
|}
|}


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