This donor completed additional genetic carrier screening that provides helpful information you can use for your family building journey!  Donor CB 556 was screened for 283 genetic conditions and was found to be a carrier for: 

• Beta-globin related hemoglobinopathies;

• Congenital adrenal hyperplasia due to 21 hydroxylase deficiency;

• Familial Mediterranean fever;

and

• Phenylalanine hydroxylase deficiency.

Please see CB 556’s test results and Additional Agreement for more information, and then simply sign the Additional Agreement for your selected donor when you place your order. 

I understand this donor has had additional genetic testing and I have read the Additional Agreement.