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"

9 matching diseasesClear search ×

Multisystem Langerhans cell histiocytosis

Multisystem Langerhans cell granulomatosis · Multisystem histiocytosis X

ORPHA:687741

Langerhans cell histiocytosis

Histiocytosis X · Langerhans cell granulomatosis

ORPHA:389

Non-Langerhans cell histiocytosis

ORPHA:157987

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: Langerhans cell histiocytosis specific to childhood

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

ORPHA:264724

Pulmonary Langerhans cell histiocytosis

Single-system pulmonary Langerhans cell histiocytosis · Single-system pulmonary histiocytosis X

ORPHA:687733

Single-system multifocal Langerhans cell histiocytosis

Single-system multifocal histiocytosis X · Single-system multifocal Langerhans cell granulomatosis

ORPHA:687738

Unifocal Langerhans cell histiocytosis

Unifocal histiocytosis X · Unifocal Langerhans cell granulomatosis

ORPHA:687730