hemochromatosis, type 3

Preferred Label : hemochromatosis, type 3;

MeSH note : Hemochromatosis due to defect in transferrin receptor 2;

MeSH synonym : hemochromatosis due to defect in transferrin receptor 2;

Details

Origin ID

C537248;

UMLS CUI

C1858664;

Currated CISMeF NLP mapping
- Hemochromatosis type 3 [ORDO Disease]
- Hemochromatosis type 3 (disorder) [SNOMED CT concept]
- Hemochromatosis, type 3 [OMIM Phenotype]
- hemochromatosis type 3 [DO Concept]
DO Cross reference
- hemochromatosis type 3 [DO Concept]
False automatic mappings
- Hemochromatosis type 1 [ORDO Disease]
MeSH term(s) associated for indexing
- hemochromatosis [MeSH Descriptor]
- receptors, transferrin [MeSH Descriptor]
ORDO relation(s)
- Hemochromatosis type 3 [ORDO Disease]
Record concept(s)
- Hemochromatosis, type 3 [MeSH concept]
See also (suggested by CISMeF)
- TFR2 protein, human [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hemochromatosis type 3 [ORDO Disease]
- Hemochromatosis type 3 (disorder) [SNOMED CT concept]
- Hemochromatosis, type 3 [OMIM Phenotype]
- hemochromatosis type 3 [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

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