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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
agammaglobulinemia +   
alpha chain disease 
autoimmune lymphoproliferative syndrome +   
Castleman disease +   
Granuloma +   
heavy chain disease +  
Immunoblastic Lymphadenopathy  
infectious mononucleosis  
Lymphangiomyoma +   
lymphoma +   
Lymphomatoid Papulosis  
lymphoplasmacytic lymphoma  
lymphoproliferative syndrome 1  
lymphoproliferative syndrome 2  
Lymphoproliferative Syndrome 3  
Macrophage Activation Syndrome  
Marek Disease 
multiple myeloma +   
mycosis fungoides +   
NATURAL KILLER CELL ENTEROPATHY  
plasmacytoma +   
Primary Cutaneous Anaplastic Large Cell Lymphoma 
primary cutaneous gamma-delta T-cell lymphoma 
sarcoidosis +   
Sezary's disease  
A form of cutaneous T-cell lymphoma manifested by generalized exfoliative ERYTHRODERMA; PRURITUS; peripheral lymphadenopathy, and abnormal hyperchromatic mononuclear (cerebriform) cells in the skin, LYMPH NODES, and peripheral blood (Sezary cells).
Tumor Lysis Syndrome  
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  
X-linked lymphoproliferative syndrome 1  
X-linked lymphoproliferative syndrome 2  

Synonyms
Exact Synonyms: Sezary Erythroderma ;   Sezary Lymphoma ;   Sezary disease ;   Sezary syndrome ;   Sezary's Lymphoma ;   Sezarys Lymphoma
Narrow Synonyms: SEZARY SYNDROME, SOMATIC
Primary IDs: MESH:D012751
Xrefs: EFO:1000785 ;   GARD:7629 ;   ICD10CM:C84.1 ;   ICD9CM:202.2 ;   NCI:C3366
Definition Sources: MESH:D012751

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