Ontology of Drug Adverse Events

Last uploaded: January 12, 2019
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Preferred Name

Hemochromatosis [Disease/Finding]
Synonyms
ID

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000001469
code

C3116
Display_Name

Hemochromatosis
imported from

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl
label

Hemochromatosis [Disease/Finding]
MeSH_CUI

M0010098
MeSH_Definition

A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron. Acquired hemochromatosis may be the result of blood transfusions, excessive dietary iron, or secondary to other disease. Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the A locus of the HLA complex on chromosome 6. (From Dorland, 27th ed)
MeSH_DUI

D006432
MeSH_Name

Hemochromatosis
NUI

N0000001469
prefixIRI

NDF-RT:N0000001469
prefLabel

Hemochromatosis [Disease/Finding]
RxNorm_CUI

1023441
SNOMED_CID

399144008

399187006
Synonym

Diabetes, Bronze
UMLS_CUI

C0018995
subClassOf

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000003902

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002006
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