GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 4
OrphanetNr:
OMIM Id: 233670
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0005512) Impaired neutrophil killing of staphylococci 3 / 7739
2
(HPO:0007499) Recurrent staphylococcal infections 3 / 7739
3
(OMIM) Neutrophil chemotaxis defect 1 / 7739
4
(OMIM) Absent neutrophil phagocytic metabolic burst 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: