Hereditary megaloblastic anaemia due to transcobalamin deficiency (Q88869): Difference between revisions
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Doença causada por absorção intestinal defeituosa de vitamina B12 devido a mutação genética autossômica recessiva. Esta doença pode se manifestar com vômitos, crescimento deficiente, infecções devido a hipogamaglobulinemia e anemia megaloblástica. | |||
| description / en | description / en | ||
A disease caused by defective intestinal absorption of vitamin B12 due to autosomal recessive genetic mutation. This disease may present with vomiting, poor growth, infections due to hypogammaglobulinemia, or megaloblastic anaemia. | |||
Revision as of 15:15, 15 August 2026
A disease caused by defective intestinal absorption of vitamin B12 due to autosomal recessive genetic mutation. This disease may present with vomiting, poor growth, infections due to hypogammaglobulinemia, or megaloblastic anaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_892302875 |
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| English | Hereditary megaloblastic anaemia due to transcobalamin deficiency |
A disease caused by defective intestinal absorption of vitamin B12 due to autosomal recessive genetic mutation. This disease may present with vomiting, poor growth, infections due to hypogammaglobulinemia, or megaloblastic anaemia. |
