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ZMYND11-gerelateerd ontwikkelingsachterstand - spraakachterstand - insulten - gedragsstoornissen - craniofaciale dysmorfie-syndroom door 10p15.3-microdeletie

ORPHA:687424· ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome due to 10p15.3 microdeletion

Overerving
Autosomal dominant