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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
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Parent Node:
expandLeukemia, T-Cell (D015458)
..Starting node
..expandLeukemia, Large Granular Lymphocytic (D054066)

       Child Nodes:



 Sister Nodes: 
..expandLeukemia, Large Granular Lymphocytic (D054066)
..expandLeukemia, Prolymphocytic, T-Cell (D015461)
..expandLeukemia-Lymphoma, Adult T-Cell (D015459)
..expandN syndrome (C536108)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6343
Name:Leukemia, Large Granular Lymphocytic
Definition:A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease.
Alternative IDs:
ParentIDs:MESH:D015458
TreeNumbers:C04.557.337.428.580.049 |C15.604.515.560.575.049 |C20.683.515.528.582.049
Synonyms:Large Granular Lymphocyte Leukemia |Leukemia, LGL |Leukemia, Lymphocytic, Large Granular |Leukemia, Natural Killer Cell Large Granular Lymphocytic |Leukemia, NK LGL |Leukemia, NK-LGL |Leukemias, LGL |Leukemias, NK-LGL |Leukemias, T-LGL |Leukemia, T Cell Large Gra
Slim Mappings:Cancer|Immune system disease|Lymphatic disease
Reference: MedGen: D054066
MeSH: D054066
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants