hemochromatosis

Preferred Label : hemochromatosis;

MedlinePlus synonym : iron overload disease;

Details

Origin ID

T1220;

UMLS CUI

C0018995;

Currated CISMeF NLP mapping
- Disorders of iron metabolism [ICD-9 code]
- HAEMOCHROMATOSIS [WHO-ART Preferred Term]
- Haemochromatosis [MedDRA Preferred Term]
- Haemochromatosis [ICD-11 More detail]
- Hemochromatosis [MedDRA LLT]
- Hemochromatosis (disorder) [Inactive SNOMED CT concept]
- Hemochromatosis (disorder) [SNOMED CT concept]
- Hemochromatosis, type 1 [OMIM Phenotype]
- Hereditary Hemochromatosis [NCIt concept]
- hemochromatosis [Radlex concept]
- hemochromatosis [DO Concept]
- hemochromatosis [Disease (Nov.)]
- hemochromatosis [MeSH Descriptor]
- hemochromatosis [MeSH concept]
- hemochromatosis [Blood Transfusion thesaurus concept]
- hemochromatosis, nos [SNOMED Notion]
MeSH descriptor(s)
- hemochromatosis [MeSH Descriptor]
See also
- blood disorders [MedlinePlus Topic]
- genetic disorders [MedlinePlus Topic]
- iron [MedlinePlus Topic]
- metabolic disorders [MedlinePlus Topic]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bronze diabetes (disorder) [SNOMED CT concept]
- Bronzed diabetes [MedDRA LLT]
- HAEMOCHROMATOSIS [WHO-ART Preferred Term]
- Haemochromatosis [MedDRA Preferred Term]
- Hemochromatosis [MedDRA LLT]
- Hemochromatosis [NCIt concept]
- Hemochromatosis (disorder) [SNOMED CT concept]
- Hereditary Hemochromatosis [NCIt concept]
- hemochromatosis [Radlex concept]
- hemochromatosis [MeSH concept]
- hemochromatosis [DO Concept]
- hemochromatosis [Disease (Nov.)]
- hemochromatosis [MeSH Descriptor]
- hemochromatosis, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- hereditary hemochromatosis [Disease (Nov.)]
Validated automatic mappings to NTBT
- Iron overload diseases [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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