OBO ID: DOID:0110869 |
Term Name: | congenital stationary night blindness 1E | Search Ontology: | |
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Synonyms: |
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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. https://www.ncbi.nlm.nih.gov/pubmed/22325361 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110869 ) |
OTHER congenital stationary night blindness 1E PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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WT + MO1-gpr179 | standard conditions | Peachey et al., 2012 |
PHENOTYPE
No data available
CITATIONS (1)
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