Term Name: Leber congenital amaurosis 17
Synonyms: LCA17
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the GDF6 gene on chromosome 8q22.
Ontology: Human Disease [DOID:0110217]   ( DOID:0110217 )

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