Search Ontology:
Human Disease

congenital stationary night blindness 1H

Term ID
DOID:0110866
Synonyms
  • congenital stationary night blindness type 1H
  • CSNB1H
Definition
A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/27063057
References
Ontology
Human Disease   ( DOID:0110866 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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