loading...| Preferred Name |
Hemochromatosis |
| Synonyms |
Troisier-Hanot-Chauffard Syndromes |
| 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 |
Troisier-Hanot-Chauffard Syndromes Hemochromatoses Von Recklenhausen-Applebaum Disease Bronze Diabetes Disorder, Iron Storage Primary Hemochromatosis Familial Hemochromatosis Recklenhausen-Applebaum Disease, Von Cirrhosis, Bronzed Cirrhoses, Pigmentary Troisier-Hanot-Chauffard Syndrome Disorders, Iron Storage Hemochromatosis, Familial Syndrome, Troisier-Hanot-Chauffard Bronzed Cirrhoses Hemochromatoses, Familial Hemochromatose Diabetes, Bronze Hemochromatosis, Genetic Cirrhoses, Bronzed Syndromes, Troisier-Hanot-Chauffard Hemochromatoses, Genetic Von Recklenhausen Applebaum Disease Recklenhausen-Applebaum Diseases, Von Haemochromatoses Storage Disorder, Iron Genetic Hemochromatoses Iron Storage Disorders Diseases, Von Recklenhausen-Applebaum Disease, Von Recklenhausen-Applebaum Pigmentary Cirrhosis Iron Storage Disorder Pigmentary Cirrhoses Familial Hemochromatoses Genetic Hemochromatosis Cirrhosis, Pigmentary Bronzed Cirrhosis Von Recklenhausen-Applebaum Diseases Troisier Hanot Chauffard Syndrome Storage Disorders, Iron Haemochromatosis |
| 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/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
| Inverse of RO | |
| Mapped from |
http://purl.bioontology.org/ontology/MESH/C537249 http://purl.bioontology.org/ontology/MESH/C537248 http://purl.bioontology.org/ontology/MESH/C566557 |
| MDA |
19990101 |
| MMR |
20130708 |
| MN |
C18.452.565.500.480 C16.320.565.618.337 C18.452.648.618.337 |
| notation |
D006432 |
| prefLabel |
Hemochromatosis |
| TERMUI |
T841564 T841566 T841568 T841571 T841573 T019431 T841565 T841569 T841567 T841570 T841574 T841572 T019432 |
| TH |
UNK (19XX) NLM (1966) NLM (2014) GHR (2014) |
| tui |
T047 |
| subClassOf |