Hereditary megaloblastic anaemia due to transcobalamin deficiency (Q88869)
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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 |
||
| 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. |
Statements
CID11:ID_892302875
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