Kongenitale Katarakt-hypertrophe Kardiomyopathie-mitochondriale Myopathie-Syndrom
ORPHA:1369· ICD-10 Q87.8· Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Infancy, Neonatal