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 ×

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

Interstitial lung disease in childhood and adulthood

ILD in childhood and adulthood

ORPHA:264757

OBSOLETE: Adult pulmonary Langerhans cell histiocytosis

OBSOLETE: Pulmonary histiocytosis X

ORPHA:99874

OBSOLETE: Eosinophilic granuloma

OBSOLETE: Chronic and localized Langerhans cell histiocytosis

ORPHA:99871

OBSOLETE: Langerhans cell histiocytosis specific to adulthood

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

ORPHA:264750

OBSOLETE: Langerhans cell histiocytosis specific to childhood

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

ORPHA:264724

OBSOLETE: Letterer-Siwe disease

OBSOLETE: Acute and disseminated Langerhans cell histiocytosis

ORPHA:99870

OBSOLETE: Sea-blue histiocytosis

ORPHA:158029

Primary interstitial lung disease in childhood and adulthood

Primary ILD in childhood and adulthood

ORPHA:264762

Secondary interstitial lung disease in childhood and adulthood

Secondary ILD in childhood and adulthood

ORPHA:264944