congenital atransferrinemia

Preferred Label : congenital atransferrinemia;

MeSH synonym : familial hypotransferrinemia; hypotransferrinemia, familial; atransferrinemia;

Origin ID

C538259;

UMLS CUI

C0521802;

CISMeF manual mappings
- Atransferrinaemia [ICD-11 More detail]
Currated CISMeF NLP mapping
- Atransferrinemia [HPO term]
- Atransferrinemia [NCIt concept]
- Atransferrinemia [OMIM Phenotype]
- Congenital atransferrinaemia [MedDRA LLT]
- Congenital atransferrinaemia [ICD-11 More detail]
- Congenital atransferrinemia [MedDRA LLT]
- Congenital atransferrinemia [ORDO Disease]
- Congenital atransferrinemia (disorder) [SNOMED CT concept]
- atransferrinemia [Disease (Nov.)]
- atransferrinemia [DO Concept]
- congenital atransferrinemia [SNOMED Notion]
HPO term
- Atransferrinemia [HPO term]
MeSH term(s) associated for indexing
- metal metabolism, inborn errors [MeSH Descriptor]
- transferrin [MeSH Descriptor]
ORDO relation(s)
- Congenital atransferrinemia [ORDO Disease]
Record concept(s)
- Congenital atransferrinemia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atransferrinaemia [ICD-11 More detail]
- Atransferrinemia [OMIM Phenotype]
- Atransferrinemia [HPO term]
- Atransferrinemia [NCIt concept]
- Congenital atransferrinaemia [MedDRA LLT]
- Congenital atransferrinemia [ORDO Disease]
- Congenital atransferrinemia [MedDRA LLT]
- Congenital atransferrinemia (disorder) [SNOMED CT concept]
- atransferrinemia [DO Concept]
- atransferrinemia [Disease (Nov.)]
- congenital atransferrinemia [SNOMED Notion]
Validated automatic mappings to NTBT
- atransferrinemia [DO Concept]