Hearing loss, autosomal recessive 116
- Synonyms
- Deafness, autosomal recessive 116
Summary
Available tests
1 test is in the database for this condition.
Clinical tests (1 available)
Molecular Genetics Tests
Clinical features
Help- Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- 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
- Global developmental delay
- Ear malformation
- Sensorineural hearing loss disorder
Sensorineural hearing loss disorder
- MedGen UID: 9164
- Concept ID: C0018784
- Finding: Disease or Syndrome
Ear malformation
- Sensorineural hearing loss disorder
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