Autosomal recessive bestrophinopathy
Summary
Available tests
Clinical features
Help- Abnormality of the eye
- Decreased light- and dark-adapted electroretinogram amplitude
Decreased light- and dark-adapted electroretinogram amplitude
- MedGen UID: 326793
- Concept ID: C1839025
- Finding: Finding
Abnormality of the eye
- Hypermetropia
Hypermetropia
- MedGen UID: 43780
- Concept ID: C0020490
- Finding: Disease or Syndrome
Abnormality of the eye
- Reduced visual acuity
Reduced visual acuity
- MedGen UID: 65889
- Concept ID: C0234632
- Finding: Finding
Abnormality of the eye
- Retinal flecks
Retinal flecks
- MedGen UID: 602327
- Concept ID: C0423414
- Finding: Finding
Abnormality of the eye
- Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy
- MedGen UID: 333564
- Concept ID: C1840457
- Finding: Finding
Abnormality of the eye
- Decreased light- and dark-adapted electroretinogram amplitude
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.