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Human Disease

Leber congenital amaurosis 4

Term ID
DOID:0110332
Synonyms
  • 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
Ontology
Human Disease   ( DOID:0110332 )
Relationships
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Genes Involved
Zebrafish Models