Hemochromatosis [hemochromatóza]
- Terms
-
bronzový diabetes
genetická hemochromatóza
hereditární hemochromatóza
pigmentová cirhóza
primární hemochromatóza
syndrom Troisierův-Hanotův-Chauffardův
Von Recklenhausenova-Applebaumova nemoc
vrozená hemochromatóza
-
Bronze Diabetes
Bronzed Cirrhosis
Diabetes, Bronze
Familial Hemochromatosis
Genetic Hemochromatosis
Haemochromatosis
Hemochromatoses
Iron Storage Disorder
Pigmentary Cirrhosis
Primary Hemochromatosis
Troisier-Hanot-Chauffard Syndrome
Von Recklenhausen-Applebaum Disease
A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
- Annotation
- accumulation of hemosiderin in tissue
- DUI
- D006432 MeSH Browser
- CUI
- M0010098
Allowable subheadings
- BL
- blood 8
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 4
- CO
- complications 26
- CN
- congenital 13
- DI
- diagnosis 82
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy 9
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 10
- EH
- ethnology
- ET
- etiology 24
- GE
- genetics 90
- HI
- history 1
- IM
- immunology 1
- ME
- metabolism 11
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 14
- PP
- physiopathology 11
- PC
- prevention & control 3
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 40
- UR
- urine
- VE
- veterinary
- VI
- virology 1
Hemochromatosis, type 3 Disease MeSH Browser
Hemochromatosis, type 4 Disease MeSH Browser
Neonatal hemochromatosis Disease MeSH Browser