hereditary hemochromatosis

Preferred Label : hereditary hemochromatosis;

Details

Origin ID

D6-31212;

UMLS CUI

C0392514;

CISMeF manual mappings
- Idiopathic hemochromatosis (disorder) [SNOMED CT concept]
- Primary hemochromatosis (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hemochromatosis type 1 [ORDO Disease]
- Hemochromatosis type 1 [PASCAL descriptor]
- Hemochromatosis, type 1 [OMIM Phenotype]
- Hereditary Hemochromatosis [NCIt concept]
- Hereditary haemochromatosis [ICD-11 More detail]
- Hereditary haemochromatosis [MedDRA Preferred Term]
- Hereditary hemochromatosis [ICD-9 code]
- Hereditary hemochromatosis [MedDRA LLT]
- Hereditary hemochromatosis (disorder) [SNOMED CT concept]
- hemochromatosis [MeSH Descriptor]
- hemochromatosis type 1 [DO Concept]
- hereditary hemochromatosis [Disease (Nov.)]
ICD-10 exact mapping(s)
- Disorders of iron metabolism [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Constitutional anemia due to iron metabolism disorder [ORDO Disease]
- Male infertility with impaired virilization due to an hypothalamic or pituitary disorder [ORDO Disease]
Metaterm(s)
- hepatology [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Hereditary hemochromatosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Hemochromatosis [NCIt concept]
- Hereditary haemochromatosis [MedDRA Preferred Term]
- Hereditary haemochromatosis [ICD-11 More detail]
- 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]
Validated automatic mappings to BTNT
- HFE-related hereditary haemochromatosis, Type 1 [ICD-11 More detail]
- Hemochromatosis type 1 (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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