OBO ID: DOID:0110869
Term Name: congenital stationary night blindness 1E Search Ontology:
Synonyms:
  • congenital stationary night blindness 1E autosomal recessive
  • CSNB1E
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12. https://www.ncbi.nlm.nih.gov/pubmed/22325361
References:
Ontology: Human Disease   ( DOID:0110869 )
Relationships
is a type of:
OTHER congenital stationary night blindness 1E PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GPR179 Night blindness, congenital stationary (complete), 1E, autosomal recessive 614565
ZEBRAFISH MODELS
Fish Conditions Citations
WT + MO1-gpr179 standard conditions Peachey et al., 2012
PHENOTYPE No data available

CITATIONS (1)
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