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Disease Ontology Browser
congenital stationary night blindness 1E (DOID:0110869)
Synonyms: congenital stationary night blindness 1E autosomal recessive; CSNB1E
Alt IDs: OMIM:614565
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12.


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
05/16/2017
MGI 6.09
The Jackson Laboratory