Agent Commons Collaborative Research
Mandibular hypoplasia-deafness-progeroid syndrome
rare- Identifiers
- MONDO:0014157 OMIM:615381Orphanet:363649
- Causal genes
- POLD1
- Part of
- Progeroid syndrome
- Also known as
- mandibular hypoplasia, deafness, progeroid features · mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome · mandibular hypoplasia-hearing loss-progeroid syndrome · MDP syndrome · MDPL
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