Morphological abnormality of the inner ear
Symptom Information:
Symptom ID: | HPO:0011390 | ||||||||
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 inner ear(HPO:0000359) Morphological abnormality of the inner ear(HPO:0011390) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Alport syndrome | (Orphanet:63) |
Apert syndrome | (Orphanet:87) |
BOR syndrome | (Orphanet:107) |
Branchio-otic syndrome | (Orphanet:52429) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CHARGE syndrome | (Orphanet:138) |
Deafness - oligodontia | (Orphanet:3230) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
EEC syndrome | (Orphanet:1896) |
Familial progressive vestibulocochlear dysfunction | (Orphanet:1767) |
Fountain syndrome | (Orphanet:3219) |
Goldenhar syndrome | (Orphanet:374) |
MELAS | (Orphanet:550) |
Noonan syndrome | (Orphanet:648) |
Norrie disease | (Orphanet:649) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Pendred syndrome | (Orphanet:705) |
Usher syndrome | (Orphanet:886) |
Usher syndrome type 1 | (Orphanet:231169) |
Usher syndrome type 2 | (Orphanet:231178) |
Usher syndrome type 3 | (Orphanet:231183) |