Search Ontology:
Human Disease
congenital stationary night blindness 1F
- Term ID
- DOID:0110864
- Synonyms
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- congenital stationary night blindness 1F autosomal recessive
- CSNB1F
- Definition
- A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23246293
- References
- Ontology
- Human Disease ( DOID:0110864 )
- is a type of
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