ORPHA:647815
Keratitis fugax hereditaria
Also called KFH, Keratoendotheliitis fugax hereditaria
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:647815 is classified under "Immunological diseases" in the Orphanet nomenclature.