Terminology Service for NFDI4Health
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Atransferrinemia

Go to external page http://purl.obolibrary.org/obo/NCIT_C125693

An extremely rare iron overload disorder caused by mutation in the structural gene for transferrin (TF gene). It is characterized by hypochromic microcytic anemia and hemosiderosis. [ ]

Term info

Label

Atransferrinemia

Synonyms
  • Atransferrinemia
  • Congenital Atransferrinemia
  • Familial Hypotransferrinemia
  • Hereditary Atransferrinemia
Preferred Name

Atransferrinemia

Semantic Type

Disease or Syndrome

UMLS CUI

C0521802

code

C125693