Zinc, elevated plasma

Preferred Label : Zinc, elevated plasma;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Albumin binding of zinc, elevated; Hyperzincemia, familial dysalbuminemic;

Inheritance : Autosomal dominant; ? albumin gene (103600) mutation;

Prefixed ID : %194470;

Details

Origin ID

194470;

UMLS CUI

C1860228;

Automatic exact mappings (from CISMeF team)
- Hyperzincemia and hypercalprotectinemia [ORDO Disease]
- Hyperzincemia and hypercalprotectinemia (disorder) [SNOMED CT concept]
- hyperzincemia and hypercalprotectinemia [MeSH Supplementary Concept]
- hyperzincemia and hypercalprotectinemia [MeSH concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Autosomal dominant inheritance [HPO term]
ORDO concept(s)
- Hyperzincemia and hypercalprotectinemia [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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