Nonsyndromic Deafness

Hearing loss that is not associated with other signs and symptoms. Most cases are due to damage to structures of the INNER EAR. More than half of congenital cases are due to genetic factors; mutations in multiple genes have been identified, including POU3F4 (OMIM: 304400), MTRNR1 (OMIM: 561000), and MT-TS1 (OMIM: 590080).

Also Known As:

Isolated Deafness; Nonsyndromic Hearing Impairment; Nonsyndromic Hearing Loss; Undifferentiated Deafness

Otorhinolaryngologic Diseases: 204
- Ear Diseases: 267
  - Hearing Disorders: 329
    - Hearing Loss: 12667
      - Deafness: 5496
        Nonsyndromic Deafness: 341
Nervous System Diseases: 14737
- Neurologic Manifestations: 7223
  - Sensation Disorders: 123
    - Hearing Disorders: 329
      - Hearing Loss: 12667
        Deafness: 5496
        Nonsyndromic Deafness: 341
Signs and Symptoms Pathological Conditions
- Signs and Symptoms
  - Neurologic Manifestations: 7223
    - Sensation Disorders: 123
      - Hearing Disorders: 329
        Hearing Loss: 12667
        Deafness: 5496
        Nonsyndromic Deafness: 341

Xiangguang Miao Selected Research

Xiangguang Miao Research Topics

Disease

Drug/Important Bio-Agent (IBA)