Hemochromatosis classification: Difference between revisions
Jump to navigation
Jump to search
Irfan Dotani (talk | contribs) No edit summary |
|||
Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Hemochromatosis}} | {{Hemochromatosis}} | ||
{{CMG}} | {{CMG}}; {{AE}} | ||
{{PleaseHelp}} | |||
==Overview== | ==Overview== | ||
==Classification== | ==Classification== | ||
Recently, a classification has been developed (with chromosome locations): | Recently, a classification has been developed (with chromosome locations): | ||
Line 22: | Line 25: | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Gastroenterology]] | |||
[[Category:Cardiology]] | |||
[[Category:Hepatology]] | |||
[[Category:Endocrinology]] | |||
[[Category:Hematology]] | |||
[[Category:Disease]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} |
Revision as of 18:01, 19 July 2016
Hemochromatosis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Hemochromatosis classification On the Web |
American Roentgen Ray Society Images of Hemochromatosis classification |
Risk calculators and risk factors for Hemochromatosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.
Overview
Classification
Recently, a classification has been developed (with chromosome locations):
Description | OMIM | Mutation | Locus |
Haemochromatosis type 1: "classical"-haemochromatosis | 235200 | HFE | 6p21.3 |
Haemochromatosis type 2A: juvenile haemochromatosis | 602390 | hemojuvelin ("HJV", also known as HFE2) | 1q21 |
Haemochromatosis type 2B: juvenile haemochromatosis | 606464 | hepcidin antimicrobial peptide (HAMP) or HFE2B | 19q13 |
Haemochromatosis type 3 | 604720 | transferrin receptor-2 (TFR2 or HFE3) | 7q22 |
Haemochromatosis type 4 autosomal dominant haemochromatosis (all others are recessive), gene mutation | 604653 | ferroportin (SLC11A3) | 2q32 |