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Cone-Rod Dystrophy 12

mutation in PROM1

Also Known As:

CORD12

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
        Cone-Rod Dystrophy 12: 1
- Hereditary Eye Diseases: 18
  - Retinitis Pigmentosa: 3975
    - Cone-Rod Dystrophy 12: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Retinitis Pigmentosa: 3975
      - Cone-Rod Dystrophy 12: 1

Related Diseases

1.	Macular Degeneration (Age-Related Maculopathy)
2.	Retinitis Pigmentosa 41
3.	Stargardt disease 4

Experts

1.	Lima de Carvalho, Jose Ronaldo: 1 article (12/2019)
2.	Mahajan, Vinit B: 1 article (12/2019)
3.	Maumenee, Irene H: 1 article (12/2019)
4.	Park, Karen Sophia: 1 article (12/2019)
5.	Ragi, Sara D: 1 article (12/2019)
6.	Tanaka, Akemi J: 1 article (12/2019)
7.	Tsang, Stephen H: 1 article (12/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Cone-Rod Dystrophy 12:

1.	Retinaldehyde (Retinal)IBA 12/01/2019 - "Mutations in PROM1 are typically associated with cone-rod dystrophy 12 (OMIM#3612657), autosomal dominant retinal macular dystrophy 2 (OMIM#608051), autosomal recessive retinitis pigmentosa 41 (OMIM#612095), and Stargardt disease 4 (OMIM#603786). "