Hiperornitinemi-hiperamonemi-homositrülinüri sendromu
ORPHA:415· ICD-10 E72.4· Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- Yaygınlık
- Unknown
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Adolescent, Adult, Childhood, Infancy, Neonatal
ORPHA:415· ICD-10 E72.4· Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome