ORPHA:572428
Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia
Also called OAS1 deficiency, OAS1-related infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:572428 is classified under "Immunological diseases" in the Orphanet nomenclature.