Term Name: Leber congenital amaurosis 3
Synonyms: LCA3
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.
Ontology: Human Disease [DOID:0110331]   ( DOID:0110331 )

Relationships
is a type of: Leber congenital amaurosis monogenic disease