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| Term | Leber congenital amaurosis 3 | ID (Ontology) | DOID:0110331 (Human Disease) |
| Definition | A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31. | ||
| Also Known As | "LCA3" | ||
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physical disorder |__Leber congenital amaurosis__ retinal disease | |__Leber congenital amaurosis__| genetic disease | |__monogenic disease___________| Leber congenital amaurosis 3 |
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monogenic disease Leber congenital amaurosis |
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ICD10CM:H35.5 MESH:C565814 MIM:604232 |
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