Leber congenital amaurosis 11
Also known as IMPDH1 Leber congenital amaurosis, LCA11, Leber congenital amaurosis caused by mutation in IMPDH1, Leber congenital amaurosis type 11+1 more
IMPDH1 Leber congenital amaurosis, LCA11, Leber congenital amaurosis caused by mutation in IMPDH1, Leber congenital amaurosis type 11, amaurosis congenita of Leber, type 11.
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.
IMPDH1 Leber congenital amaurosis, LCA11, Leber congenital amaurosis caused by mutation in IMPDH1, Leber congenital amaurosis type 11, amaurosis congenita of Leber, type 11
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.