ORPHA:892
Von Hippel-Lindau disease
Also called Familial cerebelloretinal angiomatosis, Lindau disease, VHL, Von Hippel-Lindau syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- 1-9 / 100 000 (United Kingdom)
- Rarity class
- 1-9 / 100 000
ORPHA:892 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the eye
- Hypertension
- Renal cell carcinoma
- Adrenal pheochromocytoma
- Cerebellar hemangioblastoma
- Retinal capillary hemangioma