congenital stationary night blindness 2A
Also known as CACNA1F congenital stationary night blindness, CSNB, incomplete, X-linked, congenital stationary night blindness 2A X-linked, congenital stationary night blindness caused by mutation in CACNA1F+5 more
CACNA1F congenital stationary night blindness, CSNB, incomplete, X-linked, congenital stationary night blindness 2A X-linked, congenital stationary night blindness caused by mutation in CACNA1F, congenital stationary night blindness type 2A, night blindness, congenital stationary (incomplete), 2A, X-linked, CSNB2A, night blindness, congenital stationary, type 2, night blindness, congenital stationary, type 2A.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
CACNA1F congenital stationary night blindness, CSNB, incomplete, X-linked, congenital stationary night blindness 2A X-linked, congenital stationary night blindness caused by mutation in CACNA1F, congenital stationary night blindness type 2A, night blindness, congenital stationary (incomplete), 2A, X-linked, CSNB2A, night blindness, congenital stationary, type 2, night blindness, congenital stationary, type 2A
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.