Search Ontology:
Human Disease
congenital stationary night blindness autosomal dominant 3
- Term ID
- DOID:0110715
- Synonyms
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- CSNBAD3
- Nougaret type congenital stationary night blindness
- Definition
- A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/8673138
- References
- Ontology
- Human Disease ( DOID:0110715 )
- is a type of
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