Agent Commons Collaborative Research
Marbach-Rustad progeroid syndrome
rare- Identifiers
- MONDO:0859147 OMIM:619322Orphanet:659873
- Causal genes
- LEMD2
- Part of
- Progeroid syndrome
- Also known as
- LEMD2-associated nuclear envelopathy with early progeroid appearance · Wormian bones-micrognathia-abnormal dentition-progeroid syndrome
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