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Metadata
ID	DOID:0110864
Name	congenital stationary night blindness 1F
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. https://www.ncbi.nlm.nih.gov/pubmed/23246293
Xrefs	OMIM:615058
Synonyms	congenital stationary night blindness 1F autosomal recessive [EXACT] CSNB1F [EXACT]
Parent Relationships	is_a autosomal recessive disease is_a congenital stationary night blindness