Granulomatous disease with defect in neutrophil chemotaxis

Preferred Label : Granulomatous disease with defect in neutrophil chemotaxis;

Obsolete resource : true;

Moved to : 233700; 306400;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 233670;

Details

Origin ID

233670;

UMLS CUI

C1856261;

Currated CISMeF NLP mapping
- granulomatous disease with defect in neutrophil chemotaxis [MeSH concept]
- granulomatous disease with defect in neutrophil chemotaxis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Impaired neutrophil killing of staphylococci [HPO term]
- Recurrent staphylococcal infections [HPO term]
ORDO concept(s)
- Chronic granulomatous disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- granulomatous disease with defect in neutrophil chemotaxis [MeSH Supplementary Concept]
- granulomatous disease with defect in neutrophil chemotaxis [MeSH concept]

Keyword's position in hierarchy(ies) :

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