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Transcobalamin deficiency

Disease Export to PDF
Name:
Transcobalamin deficiency
Description:
Transcobalamin deficiency (TC) is a disorder of cobalamin transport that usually presents during the first few months of life and is characterized by megaloblastic anemia, failure to thrive, vomiting, weakness and pancytopenia.
ORPHAcode:
859
Synonyms:
Inherited deficiency of transcobalamin
Transcobalamin II deficiency
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
TCN2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14