Sendromik olmayan genetik sağırlık
ORPHA:87884· ICD-10 H90.5· Rare non-syndromic genetic deafness
- Yaygınlık
- Unknown
- Kalıtım
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:87884· ICD-10 H90.5· Rare non-syndromic genetic deafness