Recurrent bacterial infections
Symptom Information:
Symptom ID: | HPO:0002718 | ||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Infections NEC(MedDRA:10021902) Recurrent bacterial infections(HPO:0002718) Immune system disorders(MedDRA:10021428) Immunodeficiency syndromes(MedDRA:10021460) Immunodeficiency disorders NEC(MedDRA:10052739) Recurrent bacterial infections(HPO:0002718) |
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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) |