Haemochromatosis type 3

Haemochromatosis type 3
Classification and external resources
OMIM 604250

Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. It exhibits an autosomal recessive inheritance pattern.[1][2][3]

References

  1. ^ Roetto A, Totaro A, Piperno A, et al. (May 2001). "New mutations inactivating transferrin receptor 2 in hemochromatosis type 3". Blood 97 (9): 2555–60. doi:10.1182/blood.V97.9.2555. PMID 11313241. http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=11313241. 
  2. ^ Roetto A, Daraio F, Alberti F, et al. (2002). "Hemochromatosis due to mutations in transferrin receptor 2". Blood Cells Mol. Dis. 29 (3): 465–70. doi:10.1006/bcmd.2002.0585. PMID 12547237. http://linkinghub.elsevier.com/retrieve/pii/S1079979602905851. 
  3. ^ Roetto A, Camaschella C (June 2005). "New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis". Best Pract Res Clin Haematol 18 (2): 235–50. doi:10.1016/j.beha.2004.09.004. PMID 15737887. http://linkinghub.elsevier.com/retrieve/pii/S1521-6926(04)00096-9. 
Transition metal
Electrolyte
Na+ and K+
see Template:Water-electrolyte imbalance and acid-base imbalance
deficiency: Hypomagnesemia

M: NUT

cof, enz, met

noco, nuvi, sysi/epon, met

drug(A8/11/12)