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Cone Dystrophy 3

Also Known As:

COD3; CORD14; Cone-Rod Dystrophy 14; Retinal Cone Dystrophy

Networked: 2 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
        Cone Dystrophy 3: 2
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - Cone Dystrophy 3: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - Cone Dystrophy 3: 2

Related Diseases

1.	Cone Dystrophy 3
2.	Retinal Degeneration
3.	Cone Dystrophy

Experts

1.	Ali, Robin R: 1 article (03/2011)
2.	Buch, Prateek K: 1 article (03/2011)
3.	Cottrill, Phillippa: 1 article (03/2011)
4.	Duran, Yanai: 1 article (03/2011)
5.	Hunt, David M: 1 article (03/2011)
6.	Michaelides, Michel: 1 article (03/2011)
7.	Mihelec, Marija: 1 article (03/2011)
8.	Pearson, Rachael A: 1 article (03/2011)
9.	West, Emma L: 1 article (03/2011)
10.	Wilkie, Susan E: 1 article (03/2011)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Cone Dystrophy 3:

1.	Guanylate Cyclase-Activating ProteinsIBA 03/28/2011 - "Cone dystrophy 3 (COD3) is a severe dominantly inherited retinal degeneration caused by missense mutations in GUCA1A, the gene encoding Guanylate Cyclase Activating Protein 1 (GCAP1). "
2.	Cyclic NucleotidesIBA 03/28/2011 - "The role of GCAP1 in controlling cyclic nucleotide levels in photoreceptors has largely been elucidated using knock-out mice, but the disease pathology in these mice cannot be extrapolated directly to COD3 as this involves altered, rather than loss of, GCAP1 function. "
3.	Guanylate Cyclase (Guanylyl Cyclase)IBA 09/01/2001 - "Mutations in the gene for guanylate cyclase-activating protein-1 (GCAP1) (GUCA1A) have been associated with autosomal dominant cone dystrophy (COD3). "