Chronic sinusitis

Symptom Information:

Symptom ID: HPO:0011109
Synonyms:
SINUSITIS, CHRONIC [HPO:0011109]
Chronic sinusitis [OMIM:Chronic sinusitis]
Sinusitis, chronic [OMIM:Sinusitis, chronic]
Chronic sinusitis [MedDRA:10009137]
Quality:
Cross references:
OMIM: "Chronic sinusitis" [OMIM:Chronic sinusitis]
OMIM: "Sinusitis, chronic" [OMIM:Sinusitis, chronic]
Is a (Direct Parents):
MedDRA Recurrent upper respiratory tract infections
HPO         Sinusitis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the paranasal sinuses(HPO:0000245)
                      Sinusitis(HPO:0000246)
                         Chronic sinusitis(HPO:0011109)
       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)
                            Chronic sinusitis(HPO:0011109)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Recurrent upper respiratory tract infections(HPO:0002788)
          Chronic sinusitis(HPO:0011109)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE (OMIM:613502)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
CILIARY DYSKINESIA, PRIMARY, 10 (OMIM:612518)
CILIARY DYSKINESIA, PRIMARY, 12 (OMIM:612650)
CILIARY DYSKINESIA, PRIMARY, 14 (OMIM:613807)
CILIARY DYSKINESIA, PRIMARY, 16 (OMIM:614017)
CILIARY DYSKINESIA, PRIMARY, 17 (OMIM:614679)
CILIARY DYSKINESIA, PRIMARY, 21 (OMIM:615294)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Hurler-Scheie syndrome (Orphanet:93476)
Immunodeficiency by defective expression of HLA class 1 (Orphanet:34592)
Joubert syndrome 21 (OMIM:615636)
Keutel syndrome (Orphanet:85202)
Primary ciliary dyskinesia - retinitis pigmentosa (Orphanet:247522)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)