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Disease Ontology Browser
congenital stationary night blindness 1C (DOID:0110867)
Synonyms: congenital stationary night blindness 1C autosomal recessive; CSNB1C
Alt IDs: OMIM:613216
Definition: A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14.


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
07/11/2017
MGI 6.10
The Jackson Laboratory