Vitamin B12 deficiency anaemia due to congenital intrinsic factor deficiency (Q97852): Difference between revisions
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A deficiência congênita de fator intrínseco é um distúrbio raro da absorção de vitamina B12, caracterizado por anemia megaloblástica e anormalidades neurológicas. | |||
| description / en | description / en | ||
Congenital intrinsic factor deficiency is a rare disorder of vitamin B12 (cobalamin) absorption that is characterised by megaloblastic anaemia and neurological abnormalities. | |||
Revision as of 14:06, 16 August 2026
Congenital intrinsic factor deficiency is a rare disorder of vitamin B12 (cobalamin) absorption that is characterised by megaloblastic anaemia and neurological abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1528646449 |
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| English | Vitamin B12 deficiency anaemia due to congenital intrinsic factor deficiency |
Congenital intrinsic factor deficiency is a rare disorder of vitamin B12 (cobalamin) absorption that is characterised by megaloblastic anaemia and neurological abnormalities. |
