Erdheim-Chester disease

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.

Also known as: Erdheim Chester Disease, Erdheim-Chester disease, lipogranulomatosis, polyostotic sclerosing histiocytosis, ECD, Erdheim Chester disease, lipoid granulomatosis

27 clinical trials for this condition and its sub-types.