ORPHA:101351
Familial isolated congenital asplenia
- 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:101351 is classified under "Immunological diseases" in the Orphanet nomenclature.