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congenital stationary night blindness 1F (DOID:0110864)
Alliance: disease page
Synonyms: congenital stationary night blindness 1F autosomal recessive; CSNB1F
Alt IDs: OMIM:615058
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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory