ORPHA:2047
Flynn-Aird syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2047 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Progressive sensorineural hearing impairment
- Myopia
- Dermal atrophy
- Rod-cone dystrophy
- Cataract
- Dementia