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| Term | Stargardt disease 3 | ID (Ontology) | DOID:0061238 (Human Disease) | |||||||||
| Definition | A stargardt disease that is characterized by macular pigmentary changes and yellow flecks and macular retinal pigment epithelium defects and has_material_basis_in heterozygous mutation in the ELOVL4 gene on chromosome 6q14. | |||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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age related macular degeneration |__Stargardt disease |__Stargardt disease 3 2 rec. |
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| Is a | Stargardt disease | ||
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External Crossreferences & Linkouts
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| MIM:600110 | |||