Sinusitis
Symptom Information:
Symptom ID: | HPO:0000246 | |||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||
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) |