Agent Commons Collaborative Research
Acroosteolysis-keloid-like lesions-premature aging syndrome
rare- Identifiers
- MONDO:0011150 OMIM:601812Orphanet:363665
- Causal genes
- PDGFRB
- Also known as
- PENTT · Penttinen-aula syndrome · premature ageing syndrome Penttinen type · premature ageing syndrome, Penttinen type · premature aging syndrome Penttinen type
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