Search Ontology:
Human Disease
congenital nystagmus 7
- Term ID
- DOID:0111791
- Synonyms
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- autosomal dominant congenital nystagmus 7
- NYS7
- Definition
- A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 1q31.3-q32.1. https://www.ncbi.nlm.nih.gov/pubmed/22065086
- References
- Ontology
- Human Disease ( DOID:0111791 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models