Recurrent upper respiratory tract infections

Symptom Information:

Symptom ID: HPO:0002788
Synonyms:
Frequent upper respiratory infections [HPO:0002788]
Frequent upper respiratory tract infections [HPO:0002788]
Recurrent upper respiratory and lower respiratory infections [HPO:0002788]
Recurrent upper respiratory infection [HPO:0002788]
Recurrent upper respiratory infections [HPO:0002788]
Upper respiratory tract infections [HPO:0002788]
Upper respiratory tract infections, recurrent [HPO:0002788]
Frequent upper respiratory infections [OMIM:Frequent upper respiratory infections]
Frequent upper respiratory tract infections [OMIM:Frequent upper respiratory tract infections]
Recurrent upper respiratory and lower respiratory infections [OMIM:Recurrent upper respiratory and lower respiratory infections]
Recurrent upper respiratory infections [OMIM:Recurrent upper respiratory infections]
Recurrent upper respiratory tract infections [OMIM:Recurrent upper respiratory tract infections]
Upper respiratory tract infections [OMIM:Upper respiratory tract infections]
Upper respiratory tract infections [MedDRA:10046309]
Upper respiratory tract infection [MedDRA:10046306]
Quality:
Cross references:
OMIM: "Frequent upper respiratory infections" [OMIM:Frequent upper respiratory infections]
OMIM: "Frequent upper respiratory tract infections" [OMIM:Frequent upper respiratory tract infections]
OMIM: "Recurrent upper respiratory and lower respiratory infections" [OMIM:Recurrent upper respiratory and lower respiratory infections]
OMIM: "Recurrent upper respiratory infections" [OMIM:Recurrent upper respiratory infections]
OMIM: "Recurrent upper respiratory tract infections" [OMIM:Recurrent upper respiratory tract infections]
OMIM: "Upper respiratory tract infections" [OMIM:Upper respiratory tract infections]
Is a (Direct Parents):
HPO         Recurrent respiratory infections
HPO         Abnormality of the nasopharynx
MedDRA Infections - pathogen unspecified
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                      Recurrent upper respiratory tract infections(HPO:0002788)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormality of the nasopharynx(HPO:0001739)
                      Recurrent upper respiratory tract infections(HPO:0002788)
             Abnormality of the pharynx(HPO:0000600)
                Abnormality of the nasopharynx(HPO:0001739)
                   Recurrent upper respiratory tract infections(HPO:0002788)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent respiratory infections(HPO:0002205)
                   Recurrent upper respiratory tract infections(HPO:0002788)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Recurrent upper respiratory tract infections(HPO:0002788)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

2p15p16.1 microdeletion syndrome (Orphanet:261349)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V (OMIM:616100)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital laryngeal web (Orphanet:2374)
Desquamative interstitial pneumonia (Orphanet:98852)
Hurler syndrome (Orphanet:93473)
Hyper-IgM syndrome type 4 (Orphanet:101091)
Hypoplasminogenemia (Orphanet:722)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Langer-Giedion syndrome (Orphanet:502)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
Ligneous conjunctivitis (Orphanet:97231)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Obesity due to congenital leptin deficiency (Orphanet:66628)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Severe combined immunodeficiency due to DCLRE1C deficiency (Orphanet:275)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
T-B+ severe combined immunodeficiency due to JAK3 deficiency (Orphanet:35078)
WHIM syndrome (Orphanet:51636)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)