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"

12 matching diseasesClear search ×

Primary interstitial lung disease specific to adulthood

Primary ILD specific to adulthood

ORPHA:264740

Interstitial lung disease specific to adulthood

ILD specific to adulthood

ORPHA:264735

Interstitial lung disease specific to childhood

ILD specific to childhood

ORPHA:264656

Interstitial lung disease specific to infancy

ILD specific to infancy

ORPHA:264694

OBSOLETE: Langerhans cell histiocytosis specific to adulthood

OBSOLETE: Langerhans cell granulomatosis specific to adulthood · OBSOLETE: Histiocytosis X specific to adulthood

ORPHA:264750

Primary interstitial lung disease in childhood and adulthood

Primary ILD in childhood and adulthood

ORPHA:264762

Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder

Primary ILD in childhood and adulthood due to alveolar structure disorder

ORPHA:264930

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

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

Secondary interstitial lung disease specific to adulthood associated with a systemic disease

Secondary ILD specific to adulthood associated with a systemic disease

ORPHA:264745