Sindrome da geni contigui-cefalopolisindattilia di Greig
ORPHA:658805· ICD-10 Q87.0· Greig cephalopolysyndactyly-contiguous gene syndrome
- Prevalenza
- <1 / 1 000 000
- Età di esordio
- Antenatal
ORPHA:658805· ICD-10 Q87.0· Greig cephalopolysyndactyly-contiguous gene syndrome