ORPHA:193
Cohen syndrome
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Antenatal, Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:193 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of speech or vocalization
- High, narrow palate
- Tooth agenesis
- Aplasia/Hypoplasia of the tongue
- Hypoplasia of the zygomatic bone
- Slender toe