Brachyolmie-Amelogenesis imperfecta-Syndrom
ORPHA:2899· ICD-10 Q76.3· Brachyolmia-amelogenesis imperfecta syndrome
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Childhood
ORPHA:2899· ICD-10 Q76.3· Brachyolmia-amelogenesis imperfecta syndrome