Search Ontology:
Human Disease

congenital stationary night blindness 2A

Term ID
DOID:0110871
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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