Search Ontology:
Human Disease
congenital stationary night blindness 1B
- Term ID
- DOID:0110865
- Synonyms
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- autosomal recessive complete congenital stationary night blindness
- congenital stationary night blindness 1B autosomal recessive
- CSNB1B
- Definition
- A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35. https://www.ncbi.nlm.nih.gov/pubmed/15781871
- References
- Ontology
- Human Disease ( DOID:0110865 )
- is a type of
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