Recurrent infections
Symptom Information:
Symptom ID: | HPO:0002719 | ||||||||||||||||||||||||||||||||||||||
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) MedDRA: Immune system disorders(MedDRA:10021428) Immunodeficiency syndromes(MedDRA:10021460) Immunodeficiency disorders NEC(MedDRA:10052739) Recurrent infections(HPO:0002719) Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Infections NEC(MedDRA:10021902) Recurrent infections(HPO:0002719) |
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Database Frequency: | 107 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
22q11.2 deletion syndrome | (Orphanet:567) |
3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA | (OMIM:616271) |
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE | (OMIM:615214) |
ALG13-CDG | (Orphanet:324422) |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:615952) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III | (OMIM:615559) |
Alpha-mannosidosis | (Orphanet:61) |
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema | (Orphanet:69088) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Aspartylglucosaminuria | (Orphanet:93) |
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
Autosomal recessive lymphoproliferative disease | (Orphanet:238505) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY | (OMIM:210550) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Beta-mannosidosis | (Orphanet:118) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Bloom syndrome | (Orphanet:125) |
C1q DEFICIENCY | (OMIM:613652) |
CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION | (OMIM:215518) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
CYSTIC DISEASE OF LUNG | (OMIM:219600) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to ORAI1 deficiency | (Orphanet:317428) |
Common variable immunodeficiency | (Orphanet:1572) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cyclic neutropenia | (Orphanet:2686) |
DIGEORGE SYNDROME | (OMIM:188400) |
DYSMYELINATION WITH JAUNDICE | (OMIM:224250) |
Dubowitz syndrome | (Orphanet:235) |
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
FADD-related immunodeficiency | (Orphanet:306550) |
FANCONI-LIKE SYNDROME | (OMIM:227850) |
Familial glucocorticoid deficiency | (Orphanet:361) |
Fucosidosis | (Orphanet:349) |
GLUCOCORTICOID DEFICIENCY 1 | (OMIM:202200) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE III | (OMIM:613960) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HISTIOCYTOSIS, FAMILIAL LIPOCHROME | (OMIM:235900) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Hypohidrotic ectodermal dysplasia with immunodeficiency | (Orphanet:98813) |
IMMUNODEFICIENCY 37 | (OMIM:616098) |
IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1 | (OMIM:243110) |
IMMUNODEFICIENCY, COMMON VARIABLE, 7 | (OMIM:614699) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2 | (OMIM:614069) |
Immunodeficiency due to a late component of complements deficiency | (Orphanet:169150) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
Joubert syndrome 10 | (OMIM:300804) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
LAZY LEUKOCYTE SYNDROME | (OMIM:150550) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS | (OMIM:613913) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
Leprechaunism | (Orphanet:508) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Lichstenstein syndrome | (Orphanet:2390) |
MEGDEL syndrome | (Orphanet:352328) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 | (OMIM:614607) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 | (OMIM:615828) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
MONOCYTE AND DENDRITIC CELL DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:614894) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Netherton syndrome | (Orphanet:634) |
Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA | (OMIM:258360) |
PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:300359) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Pearson syndrome | (Orphanet:699) |
Persistent polyclonal B-cell lymphocytosis | (Orphanet:300324) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Primary ciliary dyskinesia | (Orphanet:244) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Prolidase deficiency | (Orphanet:742) |
Recurrent infection due to specific granule deficiency | (Orphanet:169142) |
Recurrent infections associated with rare immunoglobulin isotypes deficiency | (Orphanet:183675) |
Reticular dysgenesis | (Orphanet:33355) |
Roifman syndrome | (Orphanet:353298) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES | (OMIM:615789) |
SLC35A2-CDG | (Orphanet:356961) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Shwachman-Diamond syndrome | (Orphanet:811) |
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY | (OMIM:615387) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
TUFTSIN DEFICIENCY | (OMIM:191150) |
Timothy syndrome | (Orphanet:65283) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |
WISKOTT-ALDRICH SYNDROME 2 | (OMIM:614493) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |