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Erdheim-Chester disease

rare

Erdheim-Chester disease (ECD), a non-Langerhans form of histiocytosis, is a multisystemic disease characterized by various manifestations such as skeletal involvement with bone pain, exophthalmos, diabetes insipidus, renal impairment and central nervous system (CNS) and/or cardiovascular involvement.

Identifiers
MONDO:0018153 Orphanet:35687
Part of
Non-Langerhans cell histiocytosisSyndromic disease
Also known as
ECD · Erdheim Chester Disease · lipogranulomatosis · lipoid granulomatosis · polyostotic sclerosing histiocytosis

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