Otitis media
Symptom Information:
| Symptom ID: | HPO:0000388 | ||||
| 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 ear(HPO:0000598) Abnormality of the middle ear(HPO:0000370) Otitis media(HPO:0000388) MedDRA: Ear and labyrinth disorders(MedDRA:10013993) Middle ear disorders (excl congenital)(MedDRA:10027584) Middle ear infections and inflammations(MedDRA:10027586) Otitis media(HPO:0000388) |
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| Database Frequency: | 28 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 48,XXYY syndrome | (Orphanet:10) |
| AGAMMAGLOBULINEMIA, X-LINKED | (OMIM:300755) |
| Alström syndrome | (Orphanet:64) |
| CILIARY DYSKINESIA, PRIMARY, 14 | (OMIM:613807) |
| CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
| COMBINED IMMUNODEFICIENCY, X-LINKED | (OMIM:312863) |
| Cyclic neutropenia | (Orphanet:2686) |
| Dubowitz syndrome | (Orphanet:235) |
| Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
| Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
| Hurler-Scheie syndrome | (Orphanet:93476) |
| Kostmann syndrome | (Orphanet:99749) |
| Leukocyte adhesion deficiency type II | (Orphanet:99843) |
| Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
| Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
| Nijmegen breakage syndrome | (Orphanet:647) |
| Noonan syndrome | (Orphanet:648) |
| Primary ciliary dyskinesia - retinitis pigmentosa | (Orphanet:247522) |
| Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
| Roifman syndrome | (Orphanet:353298) |
| SOTOS SYNDROME 1 | (OMIM:117550) |
| Severe combined immunodeficiency due to DCLRE1C deficiency | (Orphanet:275) |
| Severe combined immunodeficiency due to complete RAG1/2 deficiency | (Orphanet:331206) |
| Sotos syndrome | (Orphanet:821) |
| T-B+ severe combined immunodeficiency due to CD45 deficiency | (Orphanet:169157) |
| T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency | (Orphanet:169154) |
| WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
| WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |