hemochromatosis, type 4

Preferred Label : hemochromatosis, type 4;

MeSH synonym : hemochromatosis, autosomal dominant; hemochromatosis due to defect in ferroportin;

Origin ID

C537249;

UMLS CUI

C1853733;

Automatic exact mappings (from CISMeF team)
- Ferroportin disease [MedDRA LLT]
Currated CISMeF NLP mapping
- Autosomal dominant hereditary hemochromatosis (disorder) [SNOMED CT concept]
- Hemochromatosis type 4 [ORDO Disease]
- Hemochromatosis, type 4 [OMIM Phenotype]
- Non-HFE-related hereditary haemochromatosis, Type 4 [ICD-11 More detail]
- hemochromatosis type 4 [DO Concept]
DO Cross reference
- hemochromatosis type 4 [DO Concept]
MeSH term(s) associated for indexing
- cation transport proteins [MeSH Descriptor]
- hemochromatosis [MeSH Descriptor]
ORDO relation(s)
- Hemochromatosis type 4 [ORDO Disease]
Record concept(s)
- Hemochromatosis, type 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant hereditary hemochromatosis (disorder) [SNOMED CT concept]
- Ferroportin disease [MedDRA LLT]
- Hemochromatosis type 4 [ORDO Disease]
- Hemochromatosis, type 4 [OMIM Phenotype]
- Non-HFE-related hereditary haemochromatosis, Type 4 [ICD-11 More detail]
- hemochromatosis type 4 [DO Concept]