Chronic otitis media

Symptom Information:

Symptom ID: HPO:0000389
Synonyms:
Chronic ear infection [HPO:0000389]
OTITIS MEDIA, CHRONIC [HPO:0000389]
Chronic otitis media (disorder) [Orphanet:13720]
Chronic otitis media [Orphanet:13720]
Chronic ear infection [OMIM:Chronic ear infection]
Chronic otitis media [OMIM:Chronic otitis media]
Otitis media, chronic [OMIM:Otitis media, chronic]
Chronic/relapsing otitis [Orphanet:13720]
Otitis media chronic [Orphanet:13720]
Otitis media chronic [MedDRA:10033081]
Chronic atticoantral suppurative otitis media [MedDRA:10033081]
Chronic mucoid otitis media [MedDRA:10033081]
Chronic mucoid otitis media, simple or unspecified [MedDRA:10033081]
Chronic serous otitis media [MedDRA:10033081]
Chronic serous otitis media, simple or unspecified [MedDRA:10033081]
Chronic suppurative otitis media [MedDRA:10033081]
Chronic tubotympanic suppurative otitis media [MedDRA:10033081]
Other and unspecified chronic nonsuppurative otitis media [MedDRA:10033081]
Other chronic mucoid otitis media [MedDRA:10033081]
Other chronic serous otitis media [MedDRA:10033081]
Otitis media chronic NOS [MedDRA:10033081]
Otitis media serous chronic [MedDRA:10033081]
Otitis media serous chronic NOS [MedDRA:10033081]
Otitis media suppurative chronic [MedDRA:10033081]
Otitis media suppurative chronic NOS [MedDRA:10033081]
Unspecified chronic suppurative otitis media [MedDRA:10033081]
Otitis media, chronic (rare) [OMIM:Otitis media, chronic (rare)]
Quality:
Cross references:
Orphanet:13720 "Chronic/relapsing otitis" [Orphanet:13720]
OMIM: "Chronic ear infection" [OMIM:Chronic ear infection]
OMIM: "Chronic otitis media" [OMIM:Chronic otitis media]
OMIM: "Otitis media, chronic" [OMIM:Otitis media, chronic]
OMIM: "Otitis media, chronic (rare)" [OMIM:Otitis media, chronic (rare)]
UMLS:C0271441 "Chronic otitis media" [Orphanet:13720]
Is a (Direct Parents):
MedDRA Middle ear infections and inflammations
Orphanet Hearing abnormality
HPO         Otitis media
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)
                Chronic otitis media(HPO:0000389)
MedDRA:
Ear and labyrinth disorders(MedDRA:10013993)
    Middle ear disorders (excl congenital)(MedDRA:10027584)
       Middle ear infections and inflammations(MedDRA:10027586)
          Chronic otitis media(HPO:0000389)
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microduplication syndrome (Orphanet:276422)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16q24.3 microdeletion syndrome (Orphanet:261250)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
22q11.2 deletion syndrome (Orphanet:567)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
Achondroplasia (Orphanet:15)
Acro-oto-ocular syndrome (Orphanet:2980)
Alpha-mannosidosis (Orphanet:61)
Alström syndrome (Orphanet:64)
Apert syndrome (Orphanet:87)
Aspartylglucosaminuria (Orphanet:93)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive Robinow syndrome (Orphanet:1507)
BARATELA-SCOTT SYNDROME (OMIM:300881)
BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION (OMIM:613627)
Bardet-Biedl syndrome 1 (OMIM:209900 )
CHARGE syndrome (Orphanet:138)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
CILIARY DYSKINESIA, PRIMARY, 10 (OMIM:612518)
CILIARY DYSKINESIA, PRIMARY, 16 (OMIM:614017)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Catel-Manzke syndrome (Orphanet:1388)
Chronic granulomatous disease (Orphanet:379)
Cleidocranial dysplasia (Orphanet:1452)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Common variable immunodeficiency (Orphanet:1572)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Deafness - lymphedema - leukemia (Orphanet:3226)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia syndrome (Orphanet:79373)
Eosinophilic granuloma (Orphanet:99871)
Felty syndrome (Orphanet:47612)
Fragile X syndrome (Orphanet:908)
Fucosidosis (Orphanet:349)
Geleophysic dysplasia (Orphanet:2623)
Granulomatosis with polyangiitis (Orphanet:900)
Hurler-Scheie syndrome (Orphanet:93476)
Immunodeficiency by defective expression of HLA class 1 (Orphanet:34592)
Infant botulism (Orphanet:178478)
Isolated agammaglobulinemia (Orphanet:229717)
Keutel syndrome (Orphanet:85202)
Kleefstra syndrome (Orphanet:261494)
Lamellar ichthyosis (Orphanet:313)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 6 (Orphanet:583)
Oculocerebrorenal syndrome (Orphanet:534)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Recombinant 8 syndrome (Orphanet:96167)
Reticular dysgenesis (Orphanet:33355)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency (Orphanet:183660)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Smith-Magenis syndrome (Orphanet:819)
Stickler syndrome (Orphanet:828)
Williams syndrome (Orphanet:904)
Wiskott-Aldrich syndrome (Orphanet:906)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked agammaglobulinemia (Orphanet:47)