ORPHA:2145
Craniosynostosis, Herrmann-Opitz type
- Body system
- Bone diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Antenatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2145 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Hypertelorism
- Micrognathia
- Split hand
- Intrauterine growth retardation
- Micromelia
- Short stature