neutrophil immunodeficiency syndrome

Preferred Label : neutrophil immunodeficiency syndrome;

MeSH note : mutation in RAC2 gene of NAPDH oxidase;

Origin ID

C564275;

UMLS CUI

C1842398;

Currated CISMeF NLP mapping
- Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis [OMIM Phenotype]
- Neutrophil immunodeficiency syndrome [ICD-11 Sub-sub category]
- Neutrophil immunodeficiency syndrome [ORDO Disease]
- Neutrophil immunodeficiency syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- neutrophil immunodeficiency syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis [OMIM Phenotype]
- Neutrophil immunodeficiency syndrome [ORDO Disease]
- Neutrophil immunodeficiency syndrome [ICD-11 Sub-sub category]
- Neutrophil immunodeficiency syndrome (disorder) [SNOMED CT concept]
- immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis [DO Concept]