Hearing loss, autosomal dominant 76
- Synonyms
- Deafness, autosomal dominant 76
Summary
Available tests
Clinical tests (1 available)
Molecular Genetics Tests
Clinical features
Help- Abnormality of the nervous system
- Motor delay
Motor delay
- MedGen UID: 381392
- Concept ID: C1854301
- Finding: Finding
Abnormality of the nervous system
- Positive Romberg sign
Positive Romberg sign
- MedGen UID: 66017
- Concept ID: C0240914
- Finding: Finding
Abnormality of the nervous system
- Motor delay
- Ear malformation
- Abnormal vestibular function
Abnormal vestibular function
- MedGen UID: 334848
- Concept ID: C1843865
- Finding: Finding
Ear malformation
- Sensorineural hearing loss disorder
Sensorineural hearing loss disorder
- MedGen UID: 9164
- Concept ID: C0018784
- Finding: Disease or Syndrome
Ear malformation
- Abnormal vestibular function
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