Vestibular dysfunction
Symptom Information:
Symptom ID: | HPO:0001751 | ||||||||
Synonyms: |
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Quality: | |||||||||
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) Functional abnormality of the inner ear(HPO:0011389) Vestibular dysfunction(HPO:0001751) MedDRA: |
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Database Frequency: | 19 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive nonsyndromic sensorineural deafness type DFNB | (Orphanet:90636) |
DEAFNESS, AUTOSOMAL RECESSIVE 1A | (OMIM:220290) |
DEAFNESS, AUTOSOMAL RECESSIVE 1B | (OMIM:612645) |
DEAFNESS, AUTOSOMAL RECESSIVE 2 | (OMIM:600060) |
DEAFNESS, AUTOSOMAL RECESSIVE 37 | (OMIM:607821) |
DEAFNESS, AUTOSOMAL RECESSIVE 48 | (OMIM:609439) |
DEAFNESS, AUTOSOMAL RECESSIVE 84A | (OMIM:613391) |
Familial paroxysmal ataxia | (Orphanet:97) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
MELAS | (Orphanet:550) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Pendred syndrome | (Orphanet:705) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
USHER SYNDROME, TYPE ID | (OMIM:601067) |
USHER SYNDROME, TYPE IG | (OMIM:606943) |
USHER SYNDROME, TYPE IJ | (OMIM:614869) |
USHER SYNDROME, TYPE IK | (OMIM:614990) |
Usher syndrome type 3 | (Orphanet:231183) |