Seckel syndrome 1
Also known as ATR Seckel syndrome, SCKL1, Seckel syndrome 3, Seckel syndrome caused by mutation in ATR+7 more
ATR Seckel syndrome, SCKL1, Seckel syndrome 3, Seckel syndrome caused by mutation in ATR, Seckel syndrome type 1, microcephalic primordial dwarfism I, Bird-headed dwarfism, Sckl, Seckel-type dwarfism, microcephalic primordial dwarfism 1, nanocephalic dwarfism.
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.
ATR Seckel syndrome, SCKL1, Seckel syndrome 3, Seckel syndrome caused by mutation in ATR, Seckel syndrome type 1, microcephalic primordial dwarfism I, Bird-headed dwarfism, Sckl, Seckel-type dwarfism, microcephalic primordial dwarfism 1, nanocephalic dwarfism
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.