Search Ontology:
Human Disease
congenital stationary night blindness 2A
- Term ID
- DOID:0110871
- Synonyms
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- congenital stationary night blindness 2A X-linked
- Definition
- A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23. https://www.ncbi.nlm.nih.gov/pubmed/9662399
- References
- Ontology
- Human Disease ( DOID:0110871 )
- is a type of
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Genes Involved
Zebrafish Models