loading...| Preferred Name |
Stargardt disease |
|
| Synonyms |
Stargardt 1 fundus flavimaculatus juvenile onset macular degeneration Stargardt macular dystrophy Stargardt disease 1 |
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| Definitions |
Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0019353 |
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| has_exact_synonym |
Stargardt 1 fundus flavimaculatus |
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| has_narrow_synonym |
Stargardt disease 1 |
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| has_related_synonym |
juvenile onset macular degeneration Stargardt macular dystrophy |
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| label |
Stargardt disease |
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| prefixIRI |
MONDO:0019353 |
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| prefLabel |
Stargardt disease |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/181/stargardt-disease |
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| textual definition |
Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion. |
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| subClassOf |