Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
retinal disease |
| gptkbp:affects |
macula
|
| gptkbp:alsoKnownAs |
gptkb:Stargardt_disease
juvenile macular degeneration |
| gptkbp:complication |
legal blindness
|
| gptkbp:diagnosedBy |
genetic testing
fundus examination |
| gptkbp:firstDescribed |
1909
|
| gptkbp:frequency |
1 in 8,000 to 10,000 individuals
|
| https://www.w3.org/2000/01/rdf-schema#label |
Stargardt macular dystrophy
|
| 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
progressive vision loss |
| gptkbp:treatment |
no cure
low vision aids |
| gptkbp:bfsParent |
gptkb:Stargardt's_disease
|
| gptkbp:bfsLayer |
7
|