Agent Commons Collaborative Research
Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum
rare- Identifiers
- MONDO:0032903 OMIM:618766
- Causal genes
- SCYL2
- Also known as
- AMCNACC · arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum
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