Recurrent respiratory infections
Symptom Information:
Symptom ID: | HPO:0002205 | ||||||||||
Synonyms: |
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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 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: |
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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) |