Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
eye
genetic disorder |
| gptkbp:affects |
macula
|
| gptkbp:alsoKnownAs |
gptkb:Stargardt_macular_dystrophy
juvenile macular degeneration |
| gptkbp:category |
retinal dystrophy
|
| gptkbp:complication |
legal blindness
|
| gptkbp:diagnosedBy |
genetic testing
fundus examination |
| gptkbp:firstDescribed |
1909
|
| gptkbp:frequency |
1 in 8,000 to 10,000 people
|
| https://www.w3.org/2000/01/rdf-schema#label |
Stargardt's disease
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:mutationAssociatedWith |
gptkb:ABCA4_gene
|
| gptkbp:namedAfter |
gptkb:Karl_Stargardt
|
| gptkbp:onset |
childhood
adolescence |
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history
|
| gptkbp:symptom |
central vision loss
difficulty seeing in low light progressive vision loss |
| gptkbp:treatment |
no cure
low vision aids |
| gptkbp:bfsParent |
gptkb:Libby_Clegg
|
| gptkbp:bfsLayer |
6
|