5C63.0 Disorders of cobalamin metabolism or transport
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- Hereditary vitamin B12 deficiency anaemia (3A01.0)
- Neonatal vitamin B12 deficiency anaemia (3A01.1)
- Methylmalonic aciduria, vitamin B12 responsive (5C50.E0)
- Congenital or neonatal vitamin B12 deficiency anaemia (3A01.Z)
synonyms
- Disorders of cobalamin metabolism or transport
- Haptocorrin deficiency
- Transcobalamin I deficiency
- Vitamin B12-binding protein 1 deficiency
- Vitamin B12-binding alpha-globulin deficiency
- Cobalophilin deficiency
- Protein R deficiency
- TCN1 - [Transcobalamin I] deficiency
- Other genetic defects of cobalamine transport or metabolism
- Secondary non-genetic disorders of cobalamin absorption, transport or metabolism
- Unspecified disorders of cobalamin absorption, transport or metabolism
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