Term Name: Leber congenital amaurosis 14
Synonyms: LCA14
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31.
Ontology: Human Disease [DOID:0110188]   ( DOID:0110188 )

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