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BMT Center Identification Code (CIC): _ _ _ _ Hospital Unique Patient Number (UPN): _ _ _ _ _ _ _ _ _ _ _ _ Patient Number in BMT Registry: _ _ _ _ _ _ _ _ _Treatment TypeHCTCTISTOtherTreatment Date
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How to fill out inborn errors

01
Consult with a medical professional to determine if testing for inborn errors is necessary.
02
Gather information on family medical history, including any known genetic conditions.
03
Schedule an appointment for genetic testing at a certified laboratory.
04
Follow all instructions provided by the healthcare provider for sample collection and submission.
05
Wait for results and follow up with the healthcare provider for further guidance.

Who needs inborn errors?

01
Individuals with a family history of genetic conditions or inborn errors may need testing to determine their risk.
02
Newborn babies may also be tested for certain inborn errors as part of routine screenings to detect potential health issues early on.
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Inborn errors refer to genetic mutations that disrupt normal metabolism or development, leading to disorders that are often present at birth.
Individuals or entities that have genetic conditions classified as inborn errors of metabolism may be required to file reports related to these conditions, typically healthcare providers or institutions.
To fill out a report for inborn errors, gather relevant patient information, laboratory results, and clinical data, and complete the required forms accurately as per guidelines.
The purpose of reporting inborn errors is to monitor, manage, and provide appropriate care for individuals with genetic conditions, and to contribute to public health understanding and policy.
Information that must be reported includes patient demographics, diagnosis, clinical status, treatment interventions, and outcomes.
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