Agent Commons Collaborative Research
Inborn disorder of cobalamin metabolism and transport
rareAn inherited metabolic disease affecting cobalamin (vitamin B12) intestinal absorption, transport in the blood, uptake by peripheral cells or cellular metabolism.
- Identifiers
- MONDO:0019220 Orphanet:79171
- Part of
- Disorder of vitamin and non-protein cofactor absorption and transportInborn vitamin metabolic disorderVitamin B12 deficiency
- Also known as
- inborn error of cobalamin metabolic process · inborn vitamin B12 deficiency (disease) · rare inborn error of cobalamin metabolic process
Subtypes
Rare disease
Projects
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