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Retinitis Pigmentosa 29

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
        Retinitis Pigmentosa 29: 1
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - Retinitis Pigmentosa 29: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - Retinitis Pigmentosa 29: 1

Related Diseases

1.	Leber Congenital Amaurosis
2.	Usher Syndromes (Usher Syndrome)
3.	type 1D Usher syndrome

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Retinitis Pigmentosa 29:

1.

Proteins (Proteins, Gene)FDA Link

11/03/2005 - "We characterized the genomic organization of human PCDH21 and performed mutation screening in 224 patients with autosomal recessive retinitis pigmentosa, 29 patients with Leber congenital amaurosis, and 26 patients with Usher syndrome type 1. PCDH21 spans 23 kb, consists of 17 exons, and encodes a protein that shows close phylogenetic relationship to cadherin-23 (CDH23), the protein involved in Usher syndrome type 1D. "