Hereditary haemochromatosis

Preferred Label : Hereditary haemochromatosis;

ICD-11 definition : This is a hereditary disease characterized by excessive intestinal absorption of dietary iron resulting in a pathological increase in total body iron stores.;

Details

Origin ID

173494020;

UMLS CUI

C0392514;

Currated CISMeF NLP mapping
- Hereditary haemochromatosis [MedDRA Preferred Term]
- Hereditary hemochromatosis [ICD-9 code]
- Hereditary hemochromatosis [MedDRA LLT]
- Hereditary hemochromatosis (disorder) [SNOMED CT concept]
- hereditary hemochromatosis [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Hemochromatosis [NCIt concept]
- Hereditary haemochromatosis [MedDRA Preferred Term]
- Hereditary hemochromatosis [ICD-9 code]
- Hereditary hemochromatosis [MedDRA LLT]
- Hereditary hemochromatosis (disorder) [SNOMED CT concept]
- Idiopathic hemochromatosis (disorder) [SNOMED CT concept]
- Primary hemochromatosis (disorder) [SNOMED CT concept]
- familial hemochromatosis [MeSH concept]
- hereditary hemochromatosis [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients