Mikrodeletionssyndrom 12p12.1
ORPHA:313884· ICD-10 Q93.5· 12p12.1 microdeletion syndrome
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal dominant, Not applicable
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:313884· ICD-10 Q93.5· 12p12.1 microdeletion syndrome