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Atransferrinemia in Medical Definition

Atransferrinemia

Atransferrinemia Classification & external resources 2-year old Violet, a young European girl with atransferrinemia. ICD - 9 273.8 OMIM 209300 DiseasesDB 29538 Atransferrinemia is a genetic disorder in which there is...
Atransferrinemia in other areas

Atransferrinemia - Wikipedia, the free encyclopedia

Atransferrinemia, also called familial hypotransferrinemia, is an autosomal recessive metabolic disorder in which there is an absence of transferrin, a plasma protein that transports iron through the blood.

atransferrinemia.com

Congenital atransferrinemia (hypotransferrinemia) -the absence of transferrin ... Sharing Knowledge about Atransferrinemia (Hypotransferrinemia) and Apotransferrin ...

Atransferrinemia - WrongDiagnosis.com

Atransferrinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.

Atransferrinemia - WrongDiagnosis.com

Atransferrinemia symptoms, causes, diagnosis, and treatment information for ... Atransferrinemia is listed as a "rare disease" by the Office of Rare Diseases ...

atransferrinemia - definition of atransferrinemia in the Medical ...

What is atransferrinemia? Meaning of atransferrinemia medical term. What does ... atransferrinemia /atrans·fer·ri·ne·mia/ (a-trans ... atransferrinemia ...

ATRANSFERRINEMIA - Pedbase.org

acquired atransferrinemia has been reported and is thought to arise from the ... 1994 -2007 Pedbase.org. Powered by Database of Pediatrics- ATRANSFERRINEMIA ...
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