Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome
ORPHA:598603· ICD-10 Q87.8
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Childhood, Infancy, Neonatal
ORPHA:598603· ICD-10 Q87.8