Term Name:	congenital stationary night blindness 1F
Synonyms:	congenital stationary night blindness 1F autosomal recessive, CSNB1F
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.
Ontology:	Human Disease [DOID:0110864]   ( DOID:0110864 )