bn:00042773n
Noun Concept
Categories: Rare diseases, Monocyte- and macrophage-related cutaneous conditions, Diseases named for discoverer, Histiocytosis
EN
Hand-Schuller-Christian disease  Schuller-Christian disease  Hand-Schüller-Christian disease  Hand–Schüller–Christian disease  Chronic multifocal Langerhans cell histiocytosis
EN
Inflammatory histiocytosis associated with disturbance of cholesterol metabolism; occurs chiefly in young children and is characterized by cystic defects of the skull and diabetes insipidus WordNet 3.0
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EN
Inflammatory histiocytosis associated with disturbance of cholesterol metabolism; occurs chiefly in young children and is characterized by cystic defects of the skull and diabetes insipidus WordNet 3.0 & Open English WordNet
Hand–Schüller–Christian disease is part of a spectrum of disorders known as the "Langerhans cell histiocytosis". Wikipedia
A condition associated with multifocal Langerhans cell histiocytosis and a triad of exophthalmos, lytic bone lesions (often in the skull), and diabetes insipidus. Wiktionary