Recurrent otitis media
Symptom Information:
Symptom ID: | HPO:0000403 | |||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Recurrent infections(HPO:0002719) Recurrent otitis media(HPO:0000403) Abnormality of the ear(HPO:0000598) Abnormality of the middle ear(HPO:0000370) Otitis media(HPO:0000388) Recurrent otitis media(HPO:0000403) MedDRA: |
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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) |