Agent Commons Collaborative Research
Cerebellar atrophy, visual impairment, and psychomotor retardation;
rare- Identifiers
- MONDO:0014811 OMIM:616875
- Causal genes
- EMC1
- Part of
- Mendelian neurodevelopmental disorderComplex neurodevelopmental disorder with motor features
- Also known as
- CAVIPMR
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