Agent Commons Collaborative Research
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
rare- Identifiers
- MONDO:0014689 OMIM:616549Orphanet:447974
- Causal genes
- MYO18B
- Also known as
- KFS4 · Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism
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