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Descriptor English: Hemochromatosis
Descriptor Spanish: Hemocromatosis
Descriptor hemocromatosis
Entry term(s) diabetes bronceada
Scope note: Trastorno del metabolismo del hierro caracterizado por HEMOSIDEROSIS, CIRROSIS HEPÁTICA y DIABETES MELLITUS. Es producido por el depósito masivo de hierro en las células parenquimatosas tras un prolongado incremento de la absorción del mismo. (Jablonski, Dictionary of Syndromes & Eponymic Diseases, 2d ed).
Descriptor Portuguese: Hemocromatose
Descriptor French: Hémochromatose
Entry term(s): Bronze Diabetes
Bronzed Cirrhoses
Bronzed Cirrhosis
Cirrhoses, Bronzed
Cirrhoses, Pigmentary
Cirrhosis, Bronzed
Cirrhosis, Pigmentary
Diabetes, Bronze
Disease, Von Recklenhausen-Applebaum
Diseases, Von Recklenhausen-Applebaum
Disorder, Iron Storage
Disorders, Iron Storage
Familial Hemochromatoses
Familial Hemochromatosis
Genetic Hemochromatoses
Genetic Hemochromatosis
Haemochromatoses
Haemochromatosis
Hemochromatose
Hemochromatoses
Hemochromatoses, Familial
Hemochromatoses, Genetic
Hemochromatosis, Familial
Hemochromatosis, Genetic
Iron Storage Disorder
Iron Storage Disorders
Pigmentary Cirrhoses
Pigmentary Cirrhosis
Primary Hemochromatosis
Recklenhausen-Applebaum Disease, Von
Recklenhausen-Applebaum Diseases, Von
Storage Disorder, Iron
Storage Disorders, Iron
Syndrome, Troisier-Hanot-Chauffard
Syndromes, Troisier-Hanot-Chauffard
Troisier Hanot Chauffard Syndrome
Troisier-Hanot-Chauffard Syndrome
Troisier-Hanot-Chauffard Syndromes
Von Recklenhausen Applebaum Disease
Von Recklenhausen-Applebaum Disease
Von Recklenhausen-Applebaum Diseases
Tree number(s): C16.320.565.618.337
C18.452.565.500.480
C18.452.648.618.337
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D006432
Scope note: 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
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Related: Hepcidins MeSH
DeCS ID: 6582
Unique ID: D006432
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1966/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Hemochromatosis - Preferred
Concept UI M0010098
Scope note 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)
Preferred term Hemochromatosis
Entry term(s) Bronze Diabetes
Bronzed Cirrhoses
Bronzed Cirrhosis
Cirrhoses, Bronzed
Cirrhoses, Pigmentary
Cirrhosis, Bronzed
Cirrhosis, Pigmentary
Diabetes, Bronze
Disease, Von Recklenhausen-Applebaum
Diseases, Von Recklenhausen-Applebaum
Disorder, Iron Storage
Disorders, Iron Storage
Haemochromatoses
Haemochromatosis
Hemochromatose
Hemochromatoses
Iron Storage Disorder
Iron Storage Disorders
Pigmentary Cirrhoses
Pigmentary Cirrhosis
Recklenhausen-Applebaum Disease, Von
Recklenhausen-Applebaum Diseases, Von
Storage Disorder, Iron
Storage Disorders, Iron
Syndrome, Troisier-Hanot-Chauffard
Syndromes, Troisier-Hanot-Chauffard
Troisier Hanot Chauffard Syndrome
Troisier-Hanot-Chauffard Syndrome
Troisier-Hanot-Chauffard Syndromes
Von Recklenhausen Applebaum Disease
Von Recklenhausen-Applebaum Disease
Von Recklenhausen-Applebaum Diseases
Familial Hemochromatosis - Narrower
Concept UI M0584970
Preferred term Familial Hemochromatosis
Entry term(s) Familial Hemochromatoses
Genetic Hemochromatoses
Genetic Hemochromatosis
Hemochromatoses, Familial
Hemochromatoses, Genetic
Hemochromatosis, Familial
Hemochromatosis, Genetic
Primary Hemochromatosis



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