OBO ID: DOID:0110867
Term Name: congenital stationary night blindness 1C Search Ontology:
Synonyms:
  • congenital stationary night blindness 1C autosomal recessive
  • CSNB1C
Definition: A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14. https://www.ncbi.nlm.nih.gov/pubmed/19878917
References:
Ontology: Human Disease   ( DOID:0110867 )
Relationships
is a type of:
OTHER congenital stationary night blindness 1C PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TRPM1 Night blindness, congenital stationary (complete), 1C, autosomal recessive 613216
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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