loading...| Preferred Name |
Fundus flavimaculatus |
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| Synonyms |
Stargardt disease 1 |
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| Definitions |
(FFM): Autosomal recessive retinal disorder very similar to Stargardt disease. In contrast to Stargardt disease, FFM is characterized by later onset and slowly progressive course.(STGD1): A common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_248200 |
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| definition |
(FFM): Autosomal recessive retinal disorder very similar to Stargardt disease. In contrast to Stargardt disease, FFM is characterized by later onset and slowly progressive course.(STGD1): A common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. |
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| has_obo_namespace |
cell_cycle_ontology |
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| has_related_synonym |
Stargardt disease 1 |
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| id |
OMIM:248200 |
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| label |
Fundus flavimaculatus |
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| notation |
OMIM:248200 |
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| prefLabel |
Fundus flavimaculatus |
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| treeView | ||
| subClassOf |