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- Disease Information
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
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- Deficiency
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Disease Information for Retinopathy, hereditary
- Clinical Manifestations
- Signs & Symptoms
- Decreasing visual acuity
- Eye symptoms/signs
- Ophthalmoscopic/Fundoscopic exam/abnormal
- Retinal lesions
- Retinopathy signs on exam
- Vision Loss
- Demographics & Risk Factors
- Ethnic or Racial Factors
- Danish population
- Finnish population
- Northern European population/extraction
- Norwegian population
- Scandinavian population
- Swedish population
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Eye disorders/Blindness
- Sex & Age Groups
- Population/Child
- Population/Children/all
- Associated Diseases & Rule outs
- Rule Outs
- Uveitis
- Associated Disease & Complications
- Blindness
- Hereditary Blindness
- Retinopathy
- Visual acuity loss
- Disease Mechanism & Classification
- Class
- CLASS/Eyes/accessory (category)
- CLASS/Retina involvement/disorder (ex)
- Process
- PROCESS/Ethnic predilection (ex)
- PROCESS/Hereditofamilial (category)
- Synonyms
- Synonym
- Retinopathy hereditary, Synonym/Alstroem-Olsen syndrome, Synonym/Amaurosis, congenital
- Definition
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- External Links Related to Retinopathy, hereditary
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)