loading...| Preferred Name |
Hemochromatosis |
|
| Synonyms |
Genetic Hemochromatoses Disorder, Iron Storage Hemochromatosis, Genetic Troisier Hanot Chauffard Syndrome Pigmentary Cirrhoses Genetic Hemochromatosis Disease, Von Recklenhausen-Applebaum Hemochromatosis, Familial Hemochromatose Troisier-Hanot-Chauffard Syndrome Cirrhoses, Bronzed Haemochromatosis Hemochromatoses Syndromes, Troisier-Hanot-Chauffard Troisier-Hanot-Chauffard Syndromes Cirrhosis, Pigmentary Cirrhosis, Bronzed Iron Storage Disorders Bronzed Cirrhoses Disorders, Iron Storage Primary Hemochromatosis Von Recklenhausen-Applebaum Disease Familial Hemochromatoses Diabetes, Bronze Von Recklenhausen-Applebaum Diseases Haemochromatoses Iron Storage Disorder Von Recklenhausen Applebaum Disease Bronze Diabetes Cirrhoses, Pigmentary Familial Hemochromatosis Diseases, Von Recklenhausen-Applebaum Bronzed Cirrhosis Recklenhausen-Applebaum Disease, Von Syndrome, Troisier-Hanot-Chauffard Hemochromatoses, Familial Hemochromatoses, Genetic Recklenhausen-Applebaum Diseases, Von Storage Disorder, Iron Storage Disorders, Iron Pigmentary Cirrhosis |
|
| Definitions |
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) |
|
| ID |
http://purl.bioontology.org/ontology/MESH/D006432 |
|
| altLabel |
Genetic Hemochromatoses Disorder, Iron Storage Hemochromatosis, Genetic Troisier Hanot Chauffard Syndrome Pigmentary Cirrhoses Genetic Hemochromatosis Disease, Von Recklenhausen-Applebaum Hemochromatosis, Familial Hemochromatose Troisier-Hanot-Chauffard Syndrome Cirrhoses, Bronzed Haemochromatosis Hemochromatoses Syndromes, Troisier-Hanot-Chauffard Troisier-Hanot-Chauffard Syndromes Cirrhosis, Pigmentary Cirrhosis, Bronzed Iron Storage Disorders Bronzed Cirrhoses Disorders, Iron Storage Primary Hemochromatosis Von Recklenhausen-Applebaum Disease Familial Hemochromatoses Diabetes, Bronze Von Recklenhausen-Applebaum Diseases Haemochromatoses Iron Storage Disorder Von Recklenhausen Applebaum Disease Bronze Diabetes Cirrhoses, Pigmentary Familial Hemochromatosis Diseases, Von Recklenhausen-Applebaum Bronzed Cirrhosis Recklenhausen-Applebaum Disease, Von Syndrome, Troisier-Hanot-Chauffard Hemochromatoses, Familial Hemochromatoses, Genetic Recklenhausen-Applebaum Diseases, Von Storage Disorder, Iron Storage Disorders, Iron Pigmentary Cirrhosis |
|
| AN |
accumulation of hemosiderin in tissue |
|
| AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
| cui |
C0018995 C0392514 |
|
| DC |
1 |
|
| definition |
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) |
|
| DX |
19660101 |
|
| FX |
D064451 |
|
| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
| Inverse of RO | ||
| Mapped from |
http://purl.bioontology.org/ontology/MESH/C537249 http://purl.bioontology.org/ontology/MESH/C537247 http://purl.bioontology.org/ontology/MESH/C537248 |
|
| MDA |
19990101 |
|
| MMR |
20130708 |
|
| MN |
C18.452.648.618.337 C16.320.565.618.337 C18.452.565.500.480 |
|
| notation |
D006432 |
|
| prefLabel |
Hemochromatosis |
|
| TERMUI |
T841566 T841571 T841570 T841568 T841565 T841573 T841574 T841567 T841569 T841572 T841564 T019432 T019431 |
|
| TH |
NLM (1966) UNK (19XX) GHR (2014) NLM (2014) |
|
| tui |
T047 |
|
| subClassOf |