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Human Disease
Leber congenital amaurosis 4
- Term ID
- DOID:0110332
- Synonyms
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- LCA4
- Definition
- A Leber congenital amaurosis that is characterized by a relatively severe phenotype, with maculopathy and marked bone-spicule pigmentary retinopathy in most and keratoconus and cataract in a large subset and that has_material_basis_in mutation in the AIPL1 gene on chromosome 17p13. https://www.ncbi.nlm.nih.gov/pubmed/10615133
- References
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- ICD10CM:H35.5
- MESH:C565778
- MIM:604393
- Ontology
- Human Disease ( DOID:0110332 )
- is a type of
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Genes Involved
Zebrafish Models