Term Name: Leber congenital amaurosis 11
Synonyms: LCA11
Definition: A Leber congenital amaurosis that has_material_basis_in mutation n the IMPDH1 gene on chromosome 7q31.3-q32.
Ontology: Human Disease [DOID:0110216]   ( DOID:0110216 )

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