Hereditary megaloblastic anaemia due to transcobalamin deficiency (Q88869): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (4 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_892302875 | |||||||||||||||
| Property / CURIE: CID11:ID_892302875 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_892302875 | |||||||||||||||
| Property / Canary Token: dki-india-ID_892302875 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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
0 references
dki-india-ID_892302875
0 references
Concluído
0 references
13 August 2026
0 references
