Hereditary Hemochromatosis

Preferred Label : Hereditary Hemochromatosis;

NCIt synonyms : Primary Hemochromatosis;

NCIt definition : An inherited metabolic disorder characterized by iron accumulation in the tissues.;

Détails

Origin ID

C84481;

UMLS CUI

C0392514;

Automatic exact mappings (from CISMeF team)
- Disorders of iron metabolism [ICD-10 Sub-category (who)]
- Disorders of iron metabolism [ICD-10 Sub-category]
- Hemochromatosis [ACR pathology]
- Hemochromatosis [ACR pathology]
- Hemochromatosis [ACR pathology]
- hereditary hemochromatosis [Blood Transfusion thesaurus concept]
DO Cross reference
- hemochromatosis [DO Concept]
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 (disorder) [SNOMED CT concept]
- Hereditary haemochromatosis [MedDRA Preferred Term]
- Hereditary haemochromatosis [ICD-11 More detail]
- Hereditary hemochromatosis [MedDRA LLT]
- Hereditary hemochromatosis [ICD-9 code]
- Hereditary hemochromatosis (disorder) [SNOMED CT concept]
- Idiopathic hemochromatosis (disorder) [SNOMED CT concept]
- Primary hemochromatosis (disorder) [SNOMED CT concept]
- familial hemochromatosis [MeSH concept]
- hemochromatosis [Radlex concept]
- hemochromatosis [DO Concept]
- hemochromatosis [Disease (Nov.)]
- hemochromatosis [MedlinePlus Topic]
- hemochromatosis [MeSH Descriptor]
- hemochromatosis [MeSH concept]
- hemochromatosis, nos [SNOMED Notion]
- hereditary hemochromatosis [SNOMED Notion]
Validated automatic mappings to BTNT
- hereditary hemochromatosis [Disease (Nov.)]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

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