OBO ID: DOID:0110870 |
Term Name: | congenital stationary night blindness 1A | Search Ontology: | |
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Synonyms: |
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Definition: | A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4. https://www.ncbi.nlm.nih.gov/pubmed/9662400 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110870 ) |
OTHER congenital stationary night blindness 1A PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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WT + MO1-nyx | standard conditions | Peachey et al., 2012 |
PHENOTYPE
No data available
CITATIONS (1)
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