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Term:
phagocyte bactericidal dysfunction (DOID:3262)
Annotations: Rat: (31) Mouse: (30) Human: (33) Chinchilla: (31) Bonobo: (29) Dog: (30) Squirrel: (28) Pig: (31)
Parent Terms Term With Siblings Child Terms
Abnormal Neutrophil Chemotactic Response 
acidophil adenoma 
aggressive NK-cell leukemia 
Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant  
Antibody Deficiency due to Defect in CD19 
ataxia telangiectasia +   
autoimmune disease +   
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
Autoinflammation, Immunde Dysregulation, and Eosinophilia  
autosomal dominant familial periodic fever  
B cell deficiency +   
B-cell lymphoma +   
basophil adenoma 
basophilic adenocarcinoma 
C1q Deficiency  
C9 Deficiency with Dermatomyositis 
Cartilage Hair Hypoplasia Like Syndrome 
cartilage-hair hypoplasia  
Cd4+ Lymphocyte Deficiency  
CD8 Deficiency, Familial  
combined immunodeficiency +   
Combined Inflammatory and Immunologic Defect 
complement deficiency +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Davenport Donlan Syndrome 
Deltaretrovirus Infections +   
dendritic cell deficiency +   
dendritic cell sarcoma +  
dendritic cell thymoma +  
Endotoxin Hyporesponsiveness  
Eosinophilia +   
epidermodysplasia verruciformis +   
Evans Syndrome, Immunodeficiency, and Premature Immunosenescence associated with Tripeptidyl-Peptidase II Deficiency  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
familial cold autoinflammatory syndrome +   
Familial Enteropathy with Villous Edema and Immunoglobulin G2 Deficiency 
Fanconi-like syndrome  
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency 
Griscelli syndrome +   
Hepatic Venoocclusive Disease with Immunodeficiency  
hereditary neutrophilia  
human immunodeficiency virus infectious disease +   
Hypoglobulinemia and Absent B Cells 
Immune Deficiency Disease  
Immune Deficiency, Familial Variable 
IMMUNODEFICIENCY 15 +   
immunodeficiency 18  
immunodeficiency 20  
immunodeficiency 21  
immunodeficiency 27A  
immunodeficiency 27B  
immunodeficiency 28  
immunodeficiency 29  
immunodeficiency 31A  
immunodeficiency 31B  
immunodeficiency 31C  
immunodeficiency 32B  
immunodeficiency 35  
immunodeficiency 38  
immunodeficiency 39  
immunodeficiency 42  
immunodeficiency 43  
immunodeficiency 44  
immunodeficiency 45  
immunodeficiency 47  
immunodeficiency 51  
immunodeficiency 57  
immunodeficiency 65  
immunodeficiency 66  
Immunodeficiency 67  
Immunodeficiency 68  
immunodeficiency 7  
Immunodeficiency due to Defect in MAPBP-Interacting Protein  
Immunodeficiency due to Ficolin 3 Deficiency  
Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist 
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
Immunodeficiency, Gonadal Dysgenesis, and Pulmonary Fibrosis 
immunodeficiency-centromeric instability-facial anomalies syndrome +   
immunoglobulin beta deficiency 
IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY  
infectious mononucleosis  
Inosine Phosphorylase Deficiency, Immune Defect Due To 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES  
Kotzot-Richter Syndrome 
Lazy Leukocyte Syndrome  
leukocyte adhesion deficiency +   
Leukocyte Nuclear Appendages, Hereditary Prevalence of 
Leukocytosis +   
leukopenia +   
leukostasis  
Lichtenstein Syndrome 
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
Lymphoblastic Transformation, Intrinsic Defect in 
Lymphoid System Deterioration, Progressive 
Lymphokine Deficiency 
lymphopenia +   
lymphoproliferative syndrome +   
MASP2 Deficiency  
mastocytosis +   
Monocyte Esterase Deficiency  
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
NEMO Mutation with Immunodeficiency 
Neutrophil Actin Dysfunction 
Nisch syndrome  
NK cell deficiency +   
Partial Combined Immunodeficiency with Absence of HLA Determinants and Beta-2-Microglobulin from Lymphocytes 
Pelger-Huet anomaly +   
Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain 
phagocyte bactericidal dysfunction +   
Disorders in which phagocytic cells cannot kill ingested bacteria; characterized by frequent recurring infection with formulation of granulomas.
Phagocytosis, Plasma-Related Defect in 
Presentey Anomaly  
Riddle syndrome  
Roifman Syndrome  
Roifman-Chitayat Syndrome 
Schimke immuno-osseous dysplasia  
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
Specific Granule Deficiency +   
Splenic Hypoplasia  
T cell and NK cell immunodeficiency +   
T cell deficiency +   
T Cell Immunodeficiency Primary  
T-Cell OKT4 Deficiency  
Thumb Agenesis, Short Stature, and Immunodeficiency 
Tuftsin Deficiency 
Undritz Anomaly 
WHIM syndrome  
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 

Synonyms
Exact Synonyms: Phagocyte Bactericidal Dysfunctions ;   phagocytic dysfunction
Primary IDs: MESH:D010585 ;   RDO:0005184
Definition Sources: http://en.wikipedia.org/wiki/Phagocyte_bactericidal_dysfunction "DO", MESH:D010585

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.