Phagocytosis, plasma-related defect in

Preferred Label : Phagocytosis, plasma-related defect in;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive vs. dominant;

Prefixed ID : 171100;

Details

Origin ID

171100;

UMLS CUI

C1868402;

Currated CISMeF NLP mapping
- phagocytosis, Plasma-Related defect in [MeSH concept]
- phagocytosis, Plasma-Related defect in [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- phagocytosis, Plasma-Related defect in [MeSH Supplementary Concept]
- phagocytosis, Plasma-Related defect in [MeSH concept]

Keyword's position in hierarchy(ies) :

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