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3 X-Linked Cone-Rod Dystrophy

mutation in CACNA1F

Also Known As:

Cone-Rod Dystrophy, X-Linked, 3; CORDX3

Networked: 1 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
        3 X-Linked Cone-Rod Dystrophy: 1
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - 3 X-Linked Cone-Rod Dystrophy: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - X-Linked Genetic Diseases: 42
    - 3 X-Linked Cone-Rod Dystrophy: 1
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - 3 X-Linked Cone-Rod Dystrophy: 1

Related Diseases

1.	Channelopathies
2.	Eye Diseases (Eye Disease)
3.	Cone-Rod Dystrophies
4.	congenital stationary Night blindness

Experts

1.	Audo, Isabelle: 1 article (03/2014)
2.	Biel, Martin: 1 article (03/2014)
3.	Friedburg, Christoph: 1 article (03/2014)
4.	Garcia Garrido, Marina: 1 article (03/2014)
5.	Hamel, Christian: 1 article (03/2014)
6.	Haverkamp, Silke: 1 article (03/2014)
7.	Koch, Susanne: 1 article (03/2014)
8.	Krause, Stefanie: 1 article (03/2014)
9.	Lancelot, Marie-Elise: 1 article (03/2014)
10.	Lorenz, Birgit: 1 article (03/2014)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to 3 X-Linked Cone-Rod Dystrophy:

1.	L-Type Calcium Channels (Dihydropyridine Receptor)IBA 03/15/2014 - "Mutations in CACNA1F encoding the α1-subunit of the retinal Cav1.4 L-type calcium channel have been linked to Cav1.4 channelopathies including incomplete congenital stationary night blindness type 2A (CSNB2), Åland Island eye disease (AIED) and cone-rod dystrophy type 3 (CORDX3). "
2.	Retinaldehyde (Retinal)IBA 03/15/2014 - "Mutations in CACNA1F encoding the α1-subunit of the retinal Cav1.4 L-type calcium channel have been linked to Cav1.4 channelopathies including incomplete congenital stationary night blindness type 2A (CSNB2), Åland Island eye disease (AIED) and cone-rod dystrophy type 3 (CORDX3). "