ORPHA:2069
Gastrocutaneous syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Adolescent, Adult
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2069 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Hypertelorism
- Myopia
- Melanocytic nevus
- Multiple lentigines
- Hiatus hernia
- Peptic ulcer