Doyne honeycomb retinal dystrophy
- Synonyms
- DRUSEN, RADIAL, AUTOSOMAL DOMINANT; Doyne honeycomb degeneration of retina; MALATTIA LEVENTINESE
- Modes of inheritance
- Autosomal dominant inheritance (Orphanet)
Summary
Available tests
Clinical tests (28 available)
Clinical features
Help- Abnormality of the eye
- Reticular pigmentary degeneration
Reticular pigmentary degeneration
- MedGen UID: 870326
- Concept ID: C4024769
- Finding: Disease or Syndrome
Abnormality of the eye
- Retinal dystrophy
Retinal dystrophy
- MedGen UID: 208903
- Concept ID: C0854723
- Finding: Finding
Abnormality of the eye
- Visual impairment
Visual impairment
- MedGen UID: 777085
- Concept ID: C3665347
- Finding: Finding
Abnormality of the eye
- Reticular pigmentary degeneration
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.