autosomal dominant Optic atrophy and cataract

Also Known As:

Optic atrophy and cataract, autosomal dominant; Opa3, Autosomal Dominant; Optic Atrophy 3, Autosomal Dominant; Optic atrophy, cataract, and neurologic disorder

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Eye Diseases: 3522
Nervous System Diseases: 14178
- Neurodegenerative Diseases: 42472
  - Nervous System Heredodegenerative Disorders: 63
    - Hereditary Optic Atrophies: 7
      - autosomal dominant Optic atrophy and cataract: 1
- Cranial Nerve Diseases: 554
  - Optic Nerve Diseases: 2663
    - Optic Atrophy: 819
      - Hereditary Optic Atrophies: 7
        autosomal dominant Optic atrophy and cataract: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Hereditary Optic Atrophies: 7
      - autosomal dominant Optic atrophy and cataract: 1
  - Hereditary Eye Diseases: 18
    - Hereditary Optic Atrophies: 7
      - autosomal dominant Optic atrophy and cataract: 1

Experts

1.	Amati-Bonneau, P: 1 article (04/2005)
2.	Bonneau, D: 1 article (04/2005)
3.	Dubas, F: 1 article (04/2005)
4.	Malthiéry, Y: 1 article (04/2005)
5.	Reynier, P: 1 article (04/2005)
6.	Verny, C: 1 article (04/2005)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to autosomal dominant Optic atrophy and cataract:

1.	Mitochondrial Proteins (Mitochondrial Protein)IBA 04/01/2005 - "A new clinical entity is identified: autosomal dominant optic atrophy and cataract, due to a heterozygous mutation of the OPA3 gene, a nuclear gene encoding a mitochondrial protein."