OBO ID: DOID:0110866 |
Term Name: | congenital stationary night blindness 1H | Search Ontology: | |
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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 GNB3 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/27063057 | ||
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Ontology: | Human Disease ( DOID:0110866 ) |
OTHER congenital stationary night blindness 1H PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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