Recurrent sinusitis

Symptom Information:

Symptom ID: HPO:0011108
Synonyms:
Sinusitis, recurrent [HPO:0011108]
Recurrent sinusitis [OMIM:Recurrent sinusitis]
Sinusitis, recurrent [OMIM:Sinusitis, recurrent]
Quality:
Cross references:
OMIM: "Recurrent sinusitis" [OMIM:Recurrent sinusitis]
OMIM: "Sinusitis, recurrent" [OMIM:Sinusitis, recurrent]
Is a (Direct Parents):
HPO         Sinusitis
HPO         Recurrent upper respiratory tract infections
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)
                   Recurrent upper respiratory tract infections(HPO:0002788)
                      Recurrent sinusitis(HPO:0011108)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the paranasal sinuses(HPO:0000245)
                         Sinusitis(HPO:0000246)
                            Recurrent sinusitis(HPO:0011108)
       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)
                         Recurrent sinusitis(HPO:0011108)
       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)
                         Recurrent sinusitis(HPO:0011108)
             Abnormality of the skull(HPO:0000929)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the paranasal sinuses(HPO:0000245)
                      Sinusitis(HPO:0000246)
                         Recurrent sinusitis(HPO:0011108)
             Abnormality of the pharynx(HPO:0000600)
                Abnormality of the nasopharynx(HPO:0001739)
                   Recurrent upper respiratory tract infections(HPO:0002788)
                      Recurrent sinusitis(HPO:0011108)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE (OMIM:601495)
Autosomal agammaglobulinemia (Orphanet:33110)
CILIARY DYSKINESIA, PRIMARY, 10 (OMIM:612518)
CILIARY DYSKINESIA, PRIMARY, 11 (OMIM:612649)
CILIARY DYSKINESIA, PRIMARY, 18 (OMIM:614874)
CILIARY DYSKINESIA, PRIMARY, 19 (OMIM:614935)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
CILIARY DYSKINESIA, PRIMARY, 22 (OMIM:615444)
CILIARY DYSKINESIA, PRIMARY, 23 (OMIM:615451)
CILIARY DYSKINESIA, PRIMARY, 24 (OMIM:615481)
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, 5 (OMIM:608647)
CILIARY DYSKINESIA, PRIMARY, 6 (OMIM:610852)
CILIARY DYSKINESIA, PRIMARY, 9 (OMIM:612444)
Cryptosporidiosis - chronic cholangitis - liver disease (Orphanet:357329)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE III (OMIM:613960)
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, 8, WITH AUTOIMMUNITY (OMIM:614700)
Idiopathic CD4 lymphocytopenia (Orphanet:228000)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Roifman syndrome (Orphanet:353298)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)