ORPHA:2967
Haptocorrin deficiency
Also called TCI deficiency, Transcobalamin I deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adult, Elderly
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2967 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.