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ENCowden Syndrome 7 (CWS7)
Alias:
Cws7
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Cowden Syndrome 7, also known as cws7, is related to anemia, congenital dyserythropoietic, type ii. An important gene associated with Cowden Syndrome 7 is SEC23B (SEC23 Homolog B, COPII Coat Complex Component). Affiliated tissues include thyroid and breast, and related phenotypes are papillary thyroid carcinoma and macrocephaly
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MALACARDS
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