Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   large granular lymphocyte leukemia
  

Disease ID 1746
Disease large granular lymphocyte leukemia
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.
Synonym
aggressive natural killer cell leukemia
large granular lymphocytic leukaemia
large granular lymphocytic leukemia
large granular lymphocytic leukemia (disorder)
large granular lymphocytosis
leukemia, large granular lymphocytic
leukemia, large granular lymphocytic [disease/finding]
leukemia, lgl
leukemia, lymphocytic, large granular
leukemias, lgl
lgl (large granular lymphocyte) leukemia
lgl leukemia
lgl leukemias
lgll - large granular lymphocytic leukaemia
lgll - large granular lymphocytic leukemia
lymphoproliferative disease of granular lymphocytes
lymphoproliferative disease of large granular lymphocytes
DOID
UMLS
C1522378
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:37)
C0281963  |  red cell aplasia  |  5
C0034902  |  pure red cell aplasia  |  5
C0027947  |  neutropenia  |  4
C0003873  |  rheumatoid arthritis  |  3
C0023418  |  leukemia  |  3
C0024299  |  lymphoma  |  3
C0030312  |  bone marrow failure  |  2
C0003864  |  arthritis  |  2
C0042769  |  virus infection  |  2
C0021053  |  immune disorders  |  1
C0004623  |  bacterial infections  |  1
C0001815  |  bone marrow fibrosis  |  1
C0018854  |  franklin disease  |  1
C0026764  |  myeloma  |  1
C1527336  |  sjogren's syndrome  |  1
C0205969  |  malignant thymoma  |  1
C0015773  |  felty syndrome  |  1
C0023443  |  hairy cell leukemia  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0023473  |  chronic myelogenous leukemia  |  1
C0002871  |  anemia  |  1
C0040028  |  essential thrombocythemia  |  1
C0019196  |  hepatitis c  |  1
C0024314  |  lymphoproliferative disease  |  1
C0023470  |  myelogenous leukemia  |  1
C0022972  |  lambert-eaton myasthenic syndrome  |  1
C0026764  |  multiple myeloma  |  1
C0038463  |  strongyloidiasis  |  1
C0004623  |  bacterial infection  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0022972  |  myasthenic syndrome  |  1
C0040034  |  thrombocytopenia  |  1
C0007570  |  celiac disease  |  1
C0021053  |  immune disorder  |  1
C0019158  |  hepatitis  |  1
C0334634  |  mantle cell lymphoma  |  1
C0023473  |  chronic myelogenous leukemia (cml)  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
6777  |  STAT5B  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1746
Disease large granular lymphocyte leukemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:20)
HP:0012410  |  Pure red cell aplasia  |  6
HP:0001875  |  Neutropenia  |  4
HP:0001909  |  Leukemia  |  3
HP:0002665  |  Lymphoma  |  3
HP:0001370  |  Rheumatoid arthritis  |  3
HP:0001369  |  Arthritis  |  2
HP:0005528  |  Bone marrow hypoplasia  |  2
HP:0002608  |  Celiac disease  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0001903  |  Anemia  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0005506  |  Chronic myeloid leukemia  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0002633  |  Vasculitis  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0001873  |  Low platelet count  |  1
HP:0001904  |  Autoimmune neutropenia  |  1
Disease ID 1746
Disease large granular lymphocyte leukemia
Manually Symptom
UMLS  | Name(Total Manually Symptoms:7)
C0272214  |  persistent lymphocytosis
C0085273  |  parvovirus b19 infection
C0036690  |  septicemia
C0034902  |  pure red cell aplasia
C0027947  |  neutropenia
C0023443  |  hairy cell leukemia
C0004610  |  bacteremia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0034902  |  pure red cell aplasia  |  5
C0027947  |  neutropenia  |  4
C1527336  |  sjogren's syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 1746
Disease large granular lymphocyte leukemia
Case(Waiting for update.)