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"

10 matching diseasesClear search ×

Secondary interstitial lung disease in childhood and adulthood

Secondary ILD in childhood and adulthood

ORPHA:264944

Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease

CTD-ILD · Secondary ILD in childhood and adulthood associated with a connective tissue disease

ORPHA:182104

Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease

Secondary ILD in childhood and adulthood associated with a metabolic disease

ORPHA:264968

Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease

Secondary ILD in childhood and adulthood associated with a systemic disease

ORPHA:264949

Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis

Secondary ILD in childhood and adulthood associated with a systemic vasculitis

ORPHA:264973

Interstitial lung disease in childhood and adulthood

ILD in childhood and adulthood

ORPHA:264757

OBSOLETE: Langerhans cell histiocytosis in childhood and adulthood

OBSOLETE: Histiocytosis X in childhood and adulthood · OBSOLETE: Langerhans cell granulomatosis in childhood and adulthood

ORPHA:264955

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 in childhood and adulthood due to alveolar vascular disorder

Primary ILD in childhood and adulthood due to alveolar vascular disorder

ORPHA:264935