Hennekam-Beemer sendromu
ORPHA:2135· ICD-10 Q82.2· Cutaneous mastocytosis-deafness-microtia syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:2135· ICD-10 Q82.2· Cutaneous mastocytosis-deafness-microtia syndrome