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Newfoundland Rod-Cone Dystrophy

RLBP1 protein, human mutation

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
        Newfoundland Rod-Cone Dystrophy: 1
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - Newfoundland Rod-Cone Dystrophy: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - Newfoundland Rod-Cone Dystrophy: 1

Related Diseases

1.	Retinitis Pigmentosa (Pigmentary Retinopathy)
2.	Fundus Albipunctatus

Experts

1.	Glöckle, Nicola: 1 article (06/2015)
2.	Hipp, Stephanie: 1 article (06/2015)
3.	Kohl, Susanne: 1 article (06/2015)
4.	Mohr, Julia: 1 article (06/2015)
5.	Weisschuh, Nicole: 1 article (06/2015)
6.	Zobor, Ditta: 1 article (06/2015)
7.	Zobor, Gergely: 1 article (06/2015)
8.	Zrenner, Eberhart: 1 article (06/2015)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Newfoundland Rod-Cone Dystrophy:

1.	Retinaldehyde (Retinal)IBA 06/01/2015 - "Mutations in the RLBP1 gene encoding the cellular retinaldehyde-binding protein (CRALBP) cause autosomal recessive progressive retinopathy, such as retinitis punctata albescens (RPA), Bothnia-type dystrophy (BD), Newfoundland rod-cone dystrophy (NFRCD), retinitis pigmentosa (RP) and fundus albipunctatus (FA). "
2.	Carrier Proteins (Binding Protein)IBA 06/01/2015 - "Mutations in the RLBP1 gene encoding the cellular retinaldehyde-binding protein (CRALBP) cause autosomal recessive progressive retinopathy, such as retinitis punctata albescens (RPA), Bothnia-type dystrophy (BD), Newfoundland rod-cone dystrophy (NFRCD), retinitis pigmentosa (RP) and fundus albipunctatus (FA). "