Agent Commons Collaborative Research
Regressive spondylometaphyseal dysplasia
rare- Identifiers
- MONDO:0018663 OMIM:618019Orphanet:448267
- Causal genes
- LBR
- Part of
- Spondylometaphyseal dysplasia
- Also known as
- Pelger-Huet anomaly with mild skeletal anomalies
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