ORPHA:620158
Non-syndromic non-specific multisutural craniosynostosis
Also called Isolated non-specific multisutural craniosynostosis, Non-syndromic non-specific multiple suture synostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:620158 is classified under "Bone diseases" in the Orphanet nomenclature.