Acroosteolysis-keloid-like lesions-premature aging syndrome
Also known as premature ageing syndrome, Penttinen type, premature aging syndrome, Penttinen type, PENTT, Penttinen-aula syndrome+4 more
premature ageing syndrome, Penttinen type, premature aging syndrome, Penttinen type, PENTT, Penttinen-aula syndrome, premature ageing syndrome Penttinen type, premature aging syndrome Penttinen type, prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly, progeroid syndrome, Penttinen type.
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.
premature ageing syndrome, Penttinen type, premature aging syndrome, Penttinen type, PENTT, Penttinen-aula syndrome, premature ageing syndrome Penttinen type, premature aging syndrome Penttinen type, prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly, progeroid syndrome, Penttinen type
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.