Recurrent respiratory infections

Symptom Information:

Symptom ID: HPO:0002205
Synonyms:
Frequent respiratory infections [HPO:0002205]
Multiple respiratory infections [HPO:0002205]
respiratory infections, recurrent [HPO:0002205]
Susceptibility to respiratory infections [HPO:0002205]
Frequent respiratory infections [OMIM:Frequent respiratory infections]
Multiple respiratory infections [OMIM:Multiple respiratory infections]
Recurrent respiratory infections [OMIM:Recurrent respiratory infections]
Respiratory infections, recurrent [OMIM:Respiratory infections, recurrent]
Susceptibility to respiratory infections [OMIM:Susceptibility to respiratory infections]
Repeat respiratory infections [Orphanet:33900]
Quality:
Cross references:
HPO:0011947 "Respiratory tract infection" [Orphanet:33900]
Orphanet:33900 "Repeat respiratory infections" [Orphanet:33900]
OMIM: "Frequent respiratory infections" [OMIM:Frequent respiratory infections]
OMIM: "Multiple respiratory infections" [OMIM:Multiple respiratory infections]
OMIM: "Recurrent respiratory infections" [OMIM:Recurrent respiratory infections]
OMIM: "Respiratory infections, recurrent" [OMIM:Respiratory infections, recurrent]
OMIM: "Susceptibility to respiratory infections" [OMIM:Susceptibility to respiratory infections]
Is a (Direct Parents):
HPO         Recurrent infections
Orphanet Abnormality of the respiratory system
HPO         Respiratory tract infection
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 respiratory infections(HPO:0002205)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Respiratory tract infection(HPO:0011947)
                   Recurrent respiratory infections(HPO:0002205)
MedDRA:
Database Frequency: 254 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3C syndrome (Orphanet:7)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
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 7, AUTOSOMAL RECESSIVE (OMIM:615214)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Acro-oto-ocular syndrome (Orphanet:2980)
Acroosteolysis, dominant type (Orphanet:955)
Alopecia antibody deficiency (Orphanet:1006)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-mannosidosis (Orphanet:61)
Alström syndrome (Orphanet:64)
Antisynthetase syndrome (Orphanet:81)
Aortic arch defects (Orphanet:1132)
Aspartylglucosaminuria (Orphanet:93)
Ataxia - pancytopenia (Orphanet:2585)
Ataxia-telangiectasia (Orphanet:100)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency (Orphanet:331226)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Beta-mannosidosis (Orphanet:118)
Blepharophimosis-intellectual deficit syndrome, SBBYS type (Orphanet:3047)
Bloom syndrome (Orphanet:125)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Brain-lung-thyroid syndrome (Orphanet:209905)
CADASIL (Orphanet:136)
CILIARY DYSKINESIA, PRIMARY, 12 (OMIM:612650)
CILIARY DYSKINESIA, PRIMARY, 14 (OMIM:613807)
CILIARY DYSKINESIA, PRIMARY, 15 (OMIM:613808)
CILIARY DYSKINESIA, PRIMARY, 17 (OMIM:614679)
CILIARY DYSKINESIA, PRIMARY, 18 (OMIM:614874)
CILIARY DYSKINESIA, PRIMARY, 19 (OMIM:614935)
CILIARY DYSKINESIA, PRIMARY, 2 (OMIM:606763)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
CILIARY DYSKINESIA, PRIMARY, 22 (OMIM:615444)
CILIARY DYSKINESIA, PRIMARY, 23 (OMIM:615451)
CILIARY DYSKINESIA, PRIMARY, 25 (OMIM:615482)
CILIARY DYSKINESIA, PRIMARY, 26 (OMIM:615500)
CILIARY DYSKINESIA, PRIMARY, 27 (OMIM:615504)
CILIARY DYSKINESIA, PRIMARY, 28 (OMIM:615505)
CILIARY DYSKINESIA, PRIMARY, 29 (OMIM:615872)
CILIARY DYSKINESIA, PRIMARY, 3 (OMIM:608644)
CILIARY DYSKINESIA, PRIMARY, 5 (OMIM:608647)
CILIARY DYSKINESIA, PRIMARY, 6 (OMIM:610852)
CILIARY DYSKINESIA, PRIMARY, 7 (OMIM:611884)
COG4-CDG (Orphanet:263501)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Choreoacanthocytosis (Orphanet:2388)
Chronic granulomatous disease (Orphanet:379)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Chronic respiratory distress with surfactant metabolism deficiency (Orphanet:217566)
Chédiak-Higashi syndrome (Orphanet:167)
Cleidocranial dysplasia (Orphanet:1452)
Coffin-Siris syndrome (Orphanet:1465)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Combined immunodeficiency with skin granulomas (Orphanet:157949)
Common variable immunodeficiency (Orphanet:1572)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Congenital total pulmonary venous return anomaly (Orphanet:99125)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Cryptorchidism - arachnodactyly - intellectual deficit (Orphanet:1548)
Cryptosporidiosis - chronic cholangitis - liver disease (Orphanet:357329)
Cutis laxa (Orphanet:209)
Cyclic neutropenia (Orphanet:2686)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Cystic hamartoma of lung and kidney (Orphanet:2111)
Deafness - lymphedema - leukemia (Orphanet:3226)
Deafness - onychodystrophy (Orphanet:3231)
Dermatomyositis (Orphanet:221)
Diastrophic dwarfism (Orphanet:628)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Dyskeratosis congenita (Orphanet:1775)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia - blindness (Orphanet:1806)
Emanuel syndrome (Orphanet:96170)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Erythromelalgia (Orphanet:1956)
Facial dysmorphism - immunodeficiency - livedo - short stature (Orphanet:352712)
Familial dysautonomia (Orphanet:1764)
Farber lipogranulomatosis (Orphanet:333)
Felty syndrome (Orphanet:47612)
Free sialic acid storage disease (Orphanet:834)
Fucosidosis (Orphanet:349)
GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF (OMIM:137050)
GM1 gangliosidosis (Orphanet:354)
Gamma heavy-chain disease (Orphanet:100026)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Geleophysic dysplasia (Orphanet:2623)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Good syndrome (Orphanet:169105)
Granulomatosis with polyangiitis (Orphanet:900)
Hallermann-Streiff syndrome (Orphanet:2108)
Harlequin ichthyosis (Orphanet:457)
Hennekam syndrome (Orphanet:2136)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Hereditary orotic aciduria (Orphanet:30)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hyper-IgM syndrome type 2 (Orphanet:101089)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY 17 (OMIM:615607)
IMMUNODEFICIENCY 18 (OMIM:615615)
IMMUNODEFICIENCY 19 (OMIM:615617)
IMMUNODEFICIENCY 20 (OMIM:615707)
IMMUNODEFICIENCY 22 (OMIM:615758)
IMMUNODEFICIENCY 23 (OMIM:615816)
IMMUNODEFICIENCY 31C (OMIM:614162)
IMMUNODEFICIENCY 36 (OMIM:616005)
IMMUNODEFICIENCY, COMMON VARIABLE, 10 (OMIM:615577)
IMMUNODEFICIENCY, COMMON VARIABLE, 11 (OMIM:615767)
IMMUNODEFICIENCY, COMMON VARIABLE, 3 (OMIM:613493)
IMMUNODEFICIENCY, COMMON VARIABLE, 5 (OMIM:613495)
IMMUNODEFICIENCY, COMMON VARIABLE, 6 (OMIM:613496)
IMMUNODEFICIENCY, COMMON VARIABLE, 7 (OMIM:614699)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
IMMUNOGLOBULIN A DEFICIENCY 1 (OMIM:137100)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Idiopathic pulmonary alveolar proteinosis (Orphanet:747)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Immunodeficiency with natural-killer cell deficiency (Orphanet:75391)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Infantile hypophosphatasia (Orphanet:247651)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Isolated agammaglobulinemia (Orphanet:229717)
Jacobsen syndrome (Orphanet:2308)
Jeune syndrome (Orphanet:474)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
Keutel syndrome (Orphanet:85202)
Kleefstra syndrome (Orphanet:261494)
Kostmann syndrome (Orphanet:99749)
Krabbe disease (Orphanet:487)
LOC syndrome (Orphanet:2407)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Lamellar ichthyosis (Orphanet:313)
Larynx atresia (Orphanet:1202)
Leprechaunism (Orphanet:508)
Lichstenstein syndrome (Orphanet:2390)
Lipoid proteinosis (Orphanet:530)
Locked-in syndrome (Orphanet:2406)
Low birth weight - dwarfism - dysgammaglobulinemia (Orphanet:2621)
Lyell syndrome (Orphanet:537)
Lymphangioleiomyomatosis (Orphanet:538)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
MUCUS INSPISSATION OF RESPIRATORY TRACT (OMIM:253240)
Macrosomia - microphthalmia - cleft palate (Orphanet:2432)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
Monosomy 18q (Orphanet:1600)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 7 (Orphanet:584)
NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE (OMIM:616022)
Netherton syndrome (Orphanet:634)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Niemann-Pick disease type A (Orphanet:77292)
Niemann-Pick disease type B (Orphanet:77293)
Niemann-Pick disease type E (Orphanet:99022)
Nijmegen breakage syndrome (Orphanet:647)
OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI (OMIM:259270)
Oculocerebrorenal syndrome (Orphanet:534)
Opsismodysplasia (Orphanet:2746)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
PEHO syndrome (Orphanet:2836)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Papillon-Lefèvre syndrome (Orphanet:678)
Paroxysmal cold hemoglobinuria (Orphanet:90035)
Patent arterial duct (Orphanet:706)
Pelizaeus-Merzbacher disease (Orphanet:702)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Prader-Willi syndrome (Orphanet:739)
Primary ciliary dyskinesia (Orphanet:244)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Prolidase deficiency (Orphanet:742)
Proximal spinal muscular atrophy (Orphanet:70)
Proximal spinal muscular atrophy type 2 (Orphanet:83418)
Prune belly syndrome (Orphanet:2970)
Pulmonary arterial hypertension (Orphanet:182090)
Pulmonary blastoma (Orphanet:64741)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER (OMIM:614470)
RETINITIS PIGMENTOSA 6 (OMIM:312612)
Relapsing polychondritis (Orphanet:728)
Reticular dysgenesis (Orphanet:33355)
Riboflavin transporter deficiency (Orphanet:97229)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE (OMIM:608681)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Sandhoff disease (Orphanet:796)
Sanjad-Sakati syndrome (Orphanet:2323)
Severe combined immunodeficiency (Orphanet:183660)
Severe combined immunodeficiency due to CARD11 deficiency (Orphanet:357237)
Severe combined immunodeficiency due to CORO1A deficiency (Orphanet:228003)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Severe dermatitis-multiple allergies-metabolic wasting syndrome (Orphanet:369992)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 11 with or without polydactyly (OMIM:615633)
Siegler-Brewer-Carey syndrome (Orphanet:3167)
Singleton-Merten dysplasia (Orphanet:85191)
Spastic paraplegia type 2 (Orphanet:99015)
Stevens-Johnson syndrome (Orphanet:36426)
Stickler syndrome (Orphanet:828)
Susceptibility to respiratory infections associated with CD8alpha chain mutation (Orphanet:169085)
Sweet syndrome (Orphanet:3243)
THORACIC DYSOSTOSIS, ISOLATED (OMIM:187750)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Tay-Sachs disease (Orphanet:845)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Tracheobronchomegaly (Orphanet:3347)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Vici syndrome (Orphanet:1493)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
Wiskott-Aldrich syndrome (Orphanet:906)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked agammaglobulinemia (Orphanet:47)
X-linked immunoneurologic disorder (Orphanet:2571)
X-linked spinocerebellar ataxia type 3 (Orphanet:85297)
Yellow nail syndrome (Orphanet:662)
Young syndrome (Orphanet:3471)
Zlotogora-Ogur syndrome (Orphanet:3253)