Sinusitis

Symptom Information:

Symptom ID: HPO:0000246
Synonyms:
Sinusitis (disorder) [Orphanet:8780]
Sinusitis [Orphanet:8780]
Sinusitis [OMIM:Sinusitis]
Nasal congestion/sinusitis/rhinitis/rhinorrhea [Orphanet:8780]
Sinusitis [MedDRA:10040753]
Sinus infection [MedDRA:10040753]
Sinusitis NOS [MedDRA:10040753]
Pansinusitis [MedDRA:10040753]
Rhinosinusitis [MedDRA:10040753]
Maxillary sinusitis [MedDRA:10040753]
Paranasal sinus infection [MedDRA:10040753]
Sinusitis recurrent [MedDRA:10040753]
Ethmoiditis [MedDRA:10040753]
Ethmoidal sinusitis [MedDRA:10040753]
Pansinusitis [OMIM:Pansinusitis]
Nasal congestion [MedDRA:10028735]
Rhinitis (disorder) [Orphanet:8780]
Nasal congestion (finding) [Orphanet:8780]
Rhinitis [Orphanet:8780]
Rhinorrhoea [MedDRA:10039101]
Rhinorrhea [Orphanet:8780]
Snuffles (finding) [Orphanet:8780]
Rhinorrhea [OMIM:Rhinorrhea]
Quality:
Cross references:
Orphanet:8780 "Nasal congestion/sinusitis/rhinitis/rhinorrhea" [Orphanet:8780]
OMIM: "Sinusitis" [OMIM:Sinusitis]
OMIM: "Pansinusitis" [OMIM:Pansinusitis]
OMIM: "Rhinorrhea" [OMIM:Rhinorrhea]
UMLS:C0037199 "Sinusitis" [HPO:0000246]
UMLS:C0037199 "Sinusitis" [Orphanet:8780]
UMLS:C0027424 "Nasal congestion (finding)" [Orphanet:8780]
UMLS:C0035455 "Rhinitis" [Orphanet:8780]
UMLS:C1260880 "Rhinorrhea" [Orphanet:8780]
Is a (Direct Parents):
HPO         Abnormality of the paranasal sinuses
MedDRA Recurrent upper respiratory tract infections
Orphanet Abnormality of the nose
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)
       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)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Recurrent upper respiratory tract infections(HPO:0002788)
          Sinusitis(HPO:0000246)
Database Frequency: 73 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
ATAXIA-TELANGIECTASIA (OMIM:208900)
Alström syndrome (Orphanet:64)
Anisakiasis (Orphanet:1070)
Ataxia-telangiectasia (Orphanet:100)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Bloom syndrome (Orphanet:125)
Buschke-Ollendorff syndrome (Orphanet:1306)
CHARGE syndrome (Orphanet:138)
CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES (OMIM:242670)
CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA (OMIM:242680)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
CILIARY DYSKINESIA, PRIMARY, 13 (OMIM:613193)
CILIARY DYSKINESIA, PRIMARY, 15 (OMIM:613808)
CILIARY DYSKINESIA, PRIMARY, 2 (OMIM:606763)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
CILIARY DYSKINESIA, PRIMARY, 21 (OMIM:615294)
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, 6 (OMIM:610852)
COMBINED IMMUNODEFICIENCY, X-LINKED (OMIM:312863)
Chronic granulomatous disease (Orphanet:379)
Cleidocranial dysplasia (Orphanet:1452)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Common variable immunodeficiency (Orphanet:1572)
Congenital hypothyroidism (Orphanet:442)
Ectodermal dysplasia syndrome (Orphanet:79373)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Felty syndrome (Orphanet:47612)
Fragile X syndrome (Orphanet:908)
Good syndrome (Orphanet:169105)
Granulomatosis with polyangiitis (Orphanet:900)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY 20 (OMIM:615707)
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 (OMIM:242860)
Immunodeficiency by defective expression of HLA class 1 (Orphanet:34592)
Inhalational botulism (Orphanet:254504)
Isolated agammaglobulinemia (Orphanet:229717)
Keutel syndrome (Orphanet:85202)
LACRIMAL DUCT DEFECT (OMIM:149700)
MUCUS INSPISSATION OF RESPIRATORY TRACT (OMIM:253240)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Microscopic polyangiitis (Orphanet:727)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 6 (Orphanet:583)
Nijmegen breakage syndrome (Orphanet:647)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyogenic bacterial infections due to MyD88 deficiency (Orphanet:183713)
Relapsing polychondritis (Orphanet:728)
Rheumatic fever (Orphanet:3099)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Susceptibility to chronic infection by Epstein-Barr virus (Orphanet:2566)
Systemic capillary leak syndrome (Orphanet:188)
Timothy syndrome (Orphanet:65283)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked agammaglobulinemia (Orphanet:47)
Yellow nail syndrome (Orphanet:662)