Term Name: congenital stationary night blindness 1A
Synonyms: complete CSNB X-linked, congenital stationary night blindness 1A X-linked, congenital stationary night blindness with myopia, CSNB1A, hemeralopia-myopia, myopia-night blindness, NBMI
Definition: A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.
Ontology: Human Disease [DOID:0110870]   ( DOID:0110870 )

Relationships
is a type of: congenital stationary night blindness X-linked recessive disease