Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

6 matching diseasesClear search ×

Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies

Primary ILD specific to childhood due to pulmonary surfactant protein anomalies

ORPHA:100049

Interstitial lung disease specific to childhood

ILD specific to childhood

ORPHA:264656

Primary interstitial lung disease specific to adulthood

Primary ILD specific to adulthood

ORPHA:264740

Primary interstitial lung disease specific to childhood

Primary ILD specific to childhood

ORPHA:264665

Primary interstitial lung disease specific to childhood due to alveolar structure disorder

Primary ILD specific to childhood due to alveolar structure disorder

ORPHA:264670

Primary interstitial lung disease specific to childhood due to alveolar vascular disorder

Primary ILD specific to childhood due to alveolar vascular disorder

ORPHA:264683