Recurrent bacterial infections

Symptom Information:

Symptom ID: HPO:0002718
Synonyms:
Bacterial infections, recurrent [HPO:0002718]
Frequent bacterial infections [HPO:0002718]
Frequent pyogenic infections [HPO:0002718]
Increased susceptibility to bacterial infections [HPO:0002718]
Prone to bacterial infection [HPO:0002718]
Recurrent major bacterial infections [HPO:0002718]
Recurrent pyogenic infections [HPO:0002718]
Susceptibility to pyogenic infection [HPO:0002718]
Immune deficiency [Orphanet:47080]
Increased susceptibility to infections (finding) [Orphanet:47080]
Immunodeficiency disorder (disorder) [Orphanet:47080]
Increased susceptibility to infections [Orphanet:47080]
Immunologic Deficiency Syndromes [Orphanet:47080]
Bacterial infections, recurrent [OMIM:Bacterial infections, recurrent]
Frequent bacterial infections [OMIM:Frequent bacterial infections]
Frequent pyogenic infections [OMIM:Frequent pyogenic infections]
Increased susceptibility to bacterial infections [OMIM:Increased susceptibility to bacterial infections]
Recurrent bacterial infections [OMIM:Recurrent bacterial infections]
Recurrent major bacterial infections [OMIM:Recurrent major bacterial infections]
Recurrent pyogenic infections [OMIM:Recurrent pyogenic infections]
Immunodeficiency/increased susceptibility to infections/recurrent infections [Orphanet:47080]
Immunodeficiency [Orphanet:47080]
Infection susceptibility increased [Orphanet:47080]
Immunodeficiency [MedDRA:10061598]
Immunodeficiency NOS [MedDRA:10061598]
Unspecified immunity deficiency [MedDRA:10061598]
Immunocompromised [MedDRA:10061598]
Infection susceptibility increased [MedDRA:10021866]
Increased susceptibility increased [MedDRA:10021866]
Increased susceptibility to infections NOS [MedDRA:10021866]
Infectible easily [MedDRA:10021866]
Infection susceptibility incr [MedDRA:10021866]
Immunodeficiency (e.g. .0001) [OMIM:Immunodeficiency (e.g. .0001)]
No immunodeficiency [OMIM:No immunodeficiency]
Quality:
Cross references:
HPO:0002721 "Immunodeficiency" [Orphanet:47080]
HPO:0002719 "Recurrent infections" [Orphanet:47080]
Orphanet:47080 "Immunodeficiency/increased susceptibility to infections/recurrent infections" [Orphanet:47080]
OMIM: "Bacterial infections, recurrent" [OMIM:Bacterial infections, recurrent]
OMIM: "Frequent bacterial infections" [OMIM:Frequent bacterial infections]
OMIM: "Frequent pyogenic infections" [OMIM:Frequent pyogenic infections]
OMIM: "Increased susceptibility to bacterial infections" [OMIM:Increased susceptibility to bacterial infections]
OMIM: "Recurrent bacterial infections" [OMIM:Recurrent bacterial infections]
OMIM: "Recurrent major bacterial infections" [OMIM:Recurrent major bacterial infections]
OMIM: "Recurrent pyogenic infections" [OMIM:Recurrent pyogenic infections]
OMIM: "Immunodeficiency (e.g. .0001)" [OMIM:Immunodeficiency (e.g. .0001)]
OMIM: "No immunodeficiency" [OMIM:No immunodeficiency]
UMLS:C0236171 "Increased susceptibility to infections" [Orphanet:47080]
UMLS:C0021051 "Immunologic Deficiency Syndromes" [Orphanet:47080]
Is a (Direct Parents):
Orphanet Abnormality of the immune system
MedDRA Immunodeficiency disorders NEC
HPO         Recurrent infections
MedDRA Infections NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent bacterial infections(HPO:0002718)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Immunodeficiency syndromes(MedDRA:10021460)
       Immunodeficiency disorders NEC(MedDRA:10052739)
          Recurrent bacterial infections(HPO:0002718)
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Infections NEC(MedDRA:10021902)
          Recurrent bacterial infections(HPO:0002718)
Database Frequency: 75 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE (OMIM:601495)
AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE (OMIM:613500)
AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE (OMIM:613501)
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE (OMIM:613502)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
Alpha-mannosidosis (Orphanet:61)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant severe congenital neutropenia (Orphanet:486)
Autosomal recessive Kenny-Caffey syndrome (Orphanet:93324)
Autosomal recessive hyper-IgE syndrome (Orphanet:169446)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Barth syndrome (Orphanet:111)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bloom syndrome (Orphanet:125)
COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT (OMIM:216920)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Combined immunodeficiency due to STIM1 deficiency (Orphanet:317430)
Combined immunodeficiency due to STK4 deficiency (Orphanet:314689)
Complement component 3 deficiency (Orphanet:280133)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE (OMIM:233690)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I (OMIM:233700)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II (OMIM:233710)
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED (OMIM:306400)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Griscelli disease type 2 (Orphanet:79477)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hyper-IgM syndrome type 2 (Orphanet:101089)
Hyper-IgM syndrome type 3 (Orphanet:101090)
Hyper-IgM syndrome type 4 (Orphanet:101091)
Hyper-IgM syndrome type 5 (Orphanet:101092)
IMMUNE DEFICIENCY DISEASE (OMIM:242850)
IMMUNODEFICIENCY 12 (OMIM:615468)
IMMUNODEFICIENCY 36 (OMIM:616005)
IMMUNODEFICIENCY, COMMON VARIABLE, 1 (OMIM:607594)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNODEFICIENCY, COMMON VARIABLE, 3 (OMIM:613493)
IMMUNODEFICIENCY, COMMON VARIABLE, 4 (OMIM:613494)
IMMUNODEFICIENCY, COMMON VARIABLE, 5 (OMIM:613495)
IMMUNODEFICIENCY, COMMON VARIABLE, 6 (OMIM:613496)
IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES (OMIM:242870)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Immunodeficiency with factor H anomaly (Orphanet:200421)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Intellectual deficit, X-linked, Wilson type (Orphanet:85290)
Isolated agammaglobulinemia (Orphanet:229717)
Kostmann syndrome (Orphanet:99749)
Leprechaunism (Orphanet:508)
Leukocyte adhesion deficiency type III (Orphanet:99844)
MEGDEL syndrome (Orphanet:352328)
MELAS (Orphanet:550)
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS (OMIM:250460)
MYELOLYMPHATIC INSUFFICIENCY (OMIM:310350)
NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE (OMIM:616022)
NEUTROPHIL ACTIN DYSFUNCTION (OMIM:257150)
Omenn syndrome (Orphanet:39041)
Partial acquired lipodystrophy (Orphanet:79087)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Recurrent Neisseria infections due to factor D deficiency (Orphanet:169467)
SLC35A1-CDG (Orphanet:238459)
Sanjad-Sakati syndrome (Orphanet:2323)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Susceptibility to respiratory infections associated with CD8alpha chain mutation (Orphanet:169085)
Vici syndrome (Orphanet:1493)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked hyper-IgM syndrome (Orphanet:101088)
X-linked mendelian susceptibility to mycobacterial diseases (Orphanet:319605)
X-linked severe congenital neutropenia (Orphanet:86788)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 (OMIM:612541)