Morphological abnormality of the inner ear

Symptom Information:

Symptom ID: HPO:0011390
Inner ear structural anomaly [Orphanet:13480]
Structural anomalies of inner ear/cochlea/vestible/semicircular canals [Orphanet:13480]
Cross references:
Orphanet:13480 "Structural anomalies of inner ear/cochlea/vestible/semicircular canals" [Orphanet:13480]
Is a (Direct Parents):
HPO         Abnormality of the inner ear
Orphanet Abnormality of cochlea
Orphanet Hearing abnormality
HPO         Abnormal inner ear epithelium morphology
Is a (Whole tree): HPO:
    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)
Database Frequency: 21 / 7739

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)