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| Descriptor en español: |
Hemocromatosis
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| Descriptor en inglés: | Hemochromatosis | ||||||
| Descriptor en portugués: | Hemocromatose | ||||||
| Descriptor en francés: | Hémochromatose | ||||||
| Término(s) alternativo(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 |
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| Código(s) jeráquico(s): |
C16.320.565.618.337 C18.452.565.500.480 C18.452.648.618.337 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D006432 | ||||||
| Nota de alcance: | 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) |
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| Nota de indización: | accumulation of hemosiderin in tissue |
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| Calificadores permitidos: |
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 |
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| Vea también los descriptores: |
Hepcidins
MeSH | ||||||
| Identificador de DeCS: | 6582 | ||||||
| ID del Descriptor: | D006432 | ||||||
| Clasificación de la NLM: | WR 267 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/1966 | ||||||
| Fecha de entrada: | 01/01/1999 | ||||||
| Fecha de revisión: | 08/07/2013 |
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Hemochromatosis
- Concepto preferido
Familial Hemochromatosis
- Más estrecho
| UI del concepto |
M0010098 |
| Nota de alcance | 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) |
| Término preferido | Hemochromatosis |
| Término(s) alternativo(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 |
| UI del concepto |
M0584970 |
| Término preferido | Familial Hemochromatosis |
| Término(s) alternativo(s) |
Familial Hemochromatoses Genetic Hemochromatoses Genetic Hemochromatosis Hemochromatoses, Familial Hemochromatoses, Genetic Hemochromatosis, Familial Hemochromatosis, Genetic Primary Hemochromatosis |
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