MYH9-Related Disorders

A spectrum of disorders caused by mutations in the MYH9 gene (OMIM: 160775) and characterized by thrombocytopenia, large platelets, and distinct lleukocyte inclusions (Dohle-like bodies); sensorineural deafness, CATARACTS, and NEPHRITIS may also occur.

Also Known As:

Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia; Alport syndrome with macrothrombocytopenia; Autosomal Dominant Myh9 Spectrum Disorders; DFNA17; Deafness, Autosomal Dominant 17; Dohle leukocyte inclusions with giant platelets; Epstein syndrome; Fechtner syndrome; Fechtner's syndrome; MYH9 Gene-Related Autosomal Macrothrombocytopenias; MYH9-Related Disease; MYH9RD; Macrothrombocytopathy, Nephritis, and Deafness; Macrothrombocytopathy, nephritis, deafness, and leukocyte inclusions; Macrothrombocytopenia with leukocyte inclusions; May-Hegglin anomaly; Myh9-Related Disorder; Myh9-Related Macrothrombocytopenias; Sebastian platelet syndrome; Sebastian syndrome

Otorhinolaryngologic Diseases: 204
- Ear Diseases: 267
  - Hearing Disorders: 329
    - Hearing Loss: 12667
      - Sensorineural Hearing Loss: 4083
        MYH9-Related Disorders: 146
Nervous System Diseases: 14737
- Neurologic Manifestations: 7223
  - Sensation Disorders: 123
    - Hearing Disorders: 329
      - Hearing Loss: 12667
        Sensorineural Hearing Loss: 4083
        MYH9-Related Disorders: 146
Signs and Symptoms Pathological Conditions
- Signs and Symptoms
  - Neurologic Manifestations: 7223
    - Sensation Disorders: 123
      - Hearing Disorders: 329
        Hearing Loss: 12667
        Sensorineural Hearing Loss: 4083
        MYH9-Related Disorders: 146
Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Cytopenia: 2659
    - Thrombocytopenia: 27291
      - MYH9-Related Disorders: 146
  - Blood Platelet Disorders: 129
    - Thrombocytopenia: 27291
      - MYH9-Related Disorders: 146

S Nakazato Selected Research

S Nakazato Research Topics

Disease

Drug/Important Bio-Agent (IBA)