Term Name: Leber congenital amaurosis 4
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.
Ontology: Human Disease [DOID:0110332]   ( DOID:0110332 )

Relationships
is a type of: autosomal recessive disease Leber congenital amaurosis