ORPHA:636
Neurofibromatosis type 1
Also called Nonmosaic NF1, Nonmosaic neurofibromatosis type 1, Von Recklinghausen disease
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-5 / 10 000 (United Kingdom)
- Rarity class
- 1-5 / 10 000
ORPHA:636 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Plexiform neurofibroma
- Lisch nodules
- Macule
- Neoplasm of the skin
- Astrocytoma
- Abnormality of the nervous system