Analbuminemia - CISMeF

Preferred Label : Analbuminemia;

NCIt definition : A rare, autosomal recessive inherited disorder characterized by the absence or severe reduction of circulating human serum albumin.;

NCI Metathesaurus CUI : CL503128;

Details

Origin ID

C124851;

UMLS CUI

C0878666;

Currated CISMeF NLP mapping
- Analbuminemia [OMIM Phenotype]
- Analbuminemia (finding) [SNOMED CT concept]
See also inter- (CISMeF)
- Familial dysalbuminemic hyperthyroxinemia [ORDO Disease]
- Familial dysalbuminemic hyperthyroxinemia [PASCAL descriptor]
- Familial dysalbuminemic hyperthyroxinemia (disorder) [SNOMED CT concept]
- hyperthyroxinemia, familial dysalbuminemic [MeSH concept]
- hyperthyroxinemia, familial dysalbuminemic [MeSH Descriptor]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Analbuminemia [OMIM Phenotype]
- Analbuminemia (finding) [SNOMED CT concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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