Alpha-2-macroglobulin deficiency

Preferred Label : Alpha-2-macroglobulin deficiency;

Symbol : A2MD;

CISMeF acronym : A2MD;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Laboratory abnormalities : Decreased serum alpha-2 macroglobulin levels;

Prefixed ID : 614036;

Details

Origin ID

614036;

UMLS CUI

C3279661;

Automatic exact mappings (from CISMeF team)
- A2M wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- alpha-2-Macroglobulin deficiency [MeSH concept]
- alpha-2-Macroglobulin deficiency [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- alpha-2-Macroglobulin deficiency [MeSH Supplementary Concept]
- alpha-2-Macroglobulin deficiency [MeSH concept]

Keyword's position in hierarchy(ies) :

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