- Concept UI
- M0010406
- Scope Note
- A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder.
- Terms
-
Histiocytosis, Langerhans-Cell
Preferred Term
Term UI
T020013
Date01/01/1999
LexicalTag
EPO
ThesaurusID
NLM (1976)
-
Histiocytosis X
Term UI
T020012
Date01/18/1989
LexicalTag
NON
ThesaurusID
-
Histiocytosis, Generalized
Term UI
T023615
Date01/19/1989
LexicalTag
NON
ThesaurusID
NLM (1990)
-
Histiocytosis-X
Term UI
T020011
Date07/11/1975
LexicalTag
NON
ThesaurusID
UNK (19XX)
-
Langerhans Cell Histiocytosis
Term UI
T811619
Date11/15/2011
LexicalTag
NON
ThesaurusID
-
Langerhans-Cell Granulomatosis
Term UI
T020014
Date01/18/1989
LexicalTag
EPO
ThesaurusID
-
Langerhans-Cell Histiocytosis
Term UI
T705960
Date09/18/2007
LexicalTag
EPO
ThesaurusID
-
Non-Lipid Reticuloendotheliosis
Term UI
T782967
Date12/28/2010
LexicalTag
NON
ThesaurusID
-
Schueller-Christian Disease
Term UI
T018896
Date03/30/1974
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Systemic Aleukemic Reticuloendotheliosis
Term UI
T782968
Date12/28/2010
LexicalTag
NON
ThesaurusID
-
Type 2 Histiocytosis
Term UI
T782969
Date12/28/2010
LexicalTag
NON
ThesaurusID
-
Langerhans Cell Granulomatosis
Term UI
T841871
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)