Search Ontology:
Human Disease
congenital stationary night blindness autosomal dominant 2
- Term ID
- DOID:0110863
- Synonyms
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- CSNBAD2
- Rambusch type congenital stationary night blindness
- Definition
- A congenital stationary night blindness characterized by autosomal dominant inhertance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16. https://www.ncbi.nlm.nih.gov/pubmed/8075643
- References
- Ontology
- Human Disease ( DOID:0110863 )
- is a type of
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