Hypertelorismus-Hypospadie-Polysyndaktylie-Syndrom
ORPHA:2211· ICD-10 Q87.8· Hypertelorism-hypospadias-polysyndactyly syndrome
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Neonatal
ORPHA:2211· ICD-10 Q87.8· Hypertelorism-hypospadias-polysyndactyly syndrome