OBO ID: DOID:0111796 |
Term Name: | congenital nystagmus 5 | Search Ontology: | |
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Definition: | A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4. https://www.ncbi.nlm.nih.gov/pubmed/10090899 | ||
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Ontology: | Human Disease ( DOID:0111796 ) |
OTHER congenital nystagmus 5 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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