Recurrent otitis media

Symptom Information:

Symptom ID: HPO:0000403
Synonyms:
Frequent otitis media [HPO:0000403]
Multiple episodes of otitis media [HPO:0000403]
Otitis media, recurrent [HPO:0000403]
Recurrent episodes of otitis media [HPO:0000403]
Susceptibility to otitis media [HPO:0000403]
Frequent otitis media [OMIM:Frequent otitis media]
Otitis media, recurrent [OMIM:Otitis media, recurrent]
Recurrent episodes of otitis media [OMIM:Recurrent episodes of otitis media]
Recurrent otitis media [OMIM:Recurrent otitis media]
Susceptibility to otitis media [OMIM:Susceptibility to otitis media]
Otitis media, recurrent (rare) [OMIM:Otitis media, recurrent (rare)]
Quality:
Cross references:
OMIM: "Frequent otitis media" [OMIM:Frequent otitis media]
OMIM: "Otitis media, recurrent" [OMIM:Otitis media, recurrent]
OMIM: "Recurrent episodes of otitis media" [OMIM:Recurrent episodes of otitis media]
OMIM: "Recurrent otitis media" [OMIM:Recurrent otitis media]
OMIM: "Susceptibility to otitis media" [OMIM:Susceptibility to otitis media]
OMIM: "Otitis media, recurrent (rare)" [OMIM:Otitis media, recurrent (rare)]
Is a (Direct Parents):
HPO         Otitis media
HPO         Recurrent infections
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the middle ear(HPO:0000370)
             Otitis media(HPO:0000388)
                Recurrent otitis media(HPO:0000403)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent otitis media(HPO:0000403)
MedDRA:
Database Frequency: 61 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE (OMIM:613501)
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE (OMIM:613502)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
Achondroplasia (Orphanet:15)
Alström syndrome (Orphanet:64)
Autosomal agammaglobulinemia (Orphanet:33110)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
CILIARY DYSKINESIA, PRIMARY, 13 (OMIM:613193)
CILIARY DYSKINESIA, PRIMARY, 15 (OMIM:613808)
CILIARY DYSKINESIA, PRIMARY, 18 (OMIM:614874)
CILIARY DYSKINESIA, PRIMARY, 19 (OMIM:614935)
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, 26 (OMIM:615500)
CILIARY DYSKINESIA, PRIMARY, 27 (OMIM:615504)
CILIARY DYSKINESIA, PRIMARY, 28 (OMIM:615505)
CILIARY DYSKINESIA, PRIMARY, 30 (OMIM:616037)
CILIARY DYSKINESIA, PRIMARY, 5 (OMIM:608647)
CILIARY DYSKINESIA, PRIMARY, 9 (OMIM:612444)
Emanuel syndrome (Orphanet:96170)
Floating-Harbor syndrome (Orphanet:2044)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hyaluronidase deficiency (Orphanet:67041)
IMMUNODEFICIENCY 18 (OMIM:615615)
IMMUNODEFICIENCY 19 (OMIM:615617)
IMMUNODEFICIENCY 20 (OMIM:615707)
IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1 (OMIM:243110)
IMMUNODEFICIENCY, COMMON VARIABLE, 1 (OMIM:607594)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNODEFICIENCY, COMMON VARIABLE, 3 (OMIM:613493)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
Idiopathic CD4 lymphocytopenia (Orphanet:228000)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Kabuki syndrome (Orphanet:2322)
Keutel syndrome (Orphanet:85202)
Kniest dysplasia (Orphanet:485)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Leber congenital amaurosis 10 (OMIM:611755)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE (OMIM:616022)
OTITIS MEDIA, SUSCEPTIBILITY TO (OMIM:166760)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
PELGER-HUET ANOMALY (OMIM:169400)
Poikiloderma with neutropenia (Orphanet:221046)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Rabson-Mendenhall syndrome (Orphanet:769)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
TEMPLE SYNDROME (OMIM:616222)
Williams syndrome (Orphanet:904)