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Retinal Cone Dystrophy 3B

mutation in KCNV2

Also Known As:

Cone Dystrophy with Night Blindness and Supernormal Rod Responses, KCNV2-Related

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Eye Diseases: 3522
- Retinal Diseases: 3014
  - Retinal Degeneration: 4078
    - Retinal Dystrophies: 743
      - Retinitis Pigmentosa: 3975
        Retinal Cone Dystrophy 3B
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - Retinal Cone Dystrophy 3B
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - Retinal Cone Dystrophy 3B