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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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