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"

8 matching diseasesClear search ×

OBSOLETE: Langerhans cell histiocytosis specific to childhood

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

ORPHA:264724

Interstitial lung disease specific to childhood

ILD specific to childhood

ORPHA:264656

OBSOLETE: Adult pulmonary Langerhans cell histiocytosis

OBSOLETE: Pulmonary histiocytosis X

ORPHA:99874

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

OBSOLETE: Langerhans cell histiocytosis specific to adulthood

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

ORPHA:264750

OBSOLETE: Sea-blue histiocytosis

ORPHA:158029

OBSOLETE: Systemic non-Langerhans cell histiocytosis

ORPHA:240266

Primary interstitial lung disease specific to childhood

Primary ILD specific to childhood

ORPHA:264665