ORPHA:178148
Antenatal multiminicore disease with arthrogryposis multiplex congenita
- Body system
- Neurological diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Antenatal
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:178148 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Cryptorchidism
- High palate
- Dolichocephaly
- Low-set ears
- Prominent nasal bridge
- Webbed neck