OBO ID: DOID:0110871
Term Name: congenital stationary night blindness 2A Search Ontology:
Synonyms:
  • congenital stationary night blindness 2A X-linked
Definition: A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23. https://www.ncbi.nlm.nih.gov/pubmed/9662399
References:
Ontology: Human Disease   ( DOID:0110871 )
Relationships
is a type of:
OTHER congenital stationary night blindness 2A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA1F Night blindness, congenital stationary (incomplete), 2A, X-linked 300071
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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