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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   myeloid sarcoma
  

Disease ID 1312
Disease myeloid sarcoma
Definition
An extramedullary tumor of immature MYELOID CELLS or MYELOBLASTS. Granulocytic sarcoma usually occurs with or follows the onset of ACUTE MYELOID LEUKEMIA.
Synonym
[m]chloroma
[m]granulocytic sarcoma
[m]myeloid sarcoma
cancer, green
chloroleukemia
chloroma
chloroma (disorder)
chloromas
chloromyeloma
chlorosarcoma
extramedullary myeloid cell tumor
extramedullary myeloid tumor
granulocytic sarcoma
granulocytic sarcoma (disorder)
granulocytic sarcomas
myeloid cell tumor, extramedullary
myeloid sarcoma nos
myeloid sarcoma nos (disorder)
myeloid sarcoma, disease
myeloid sarcoma, disease (disorder)
myeloid sarcoma, morphology
myeloid sarcoma, morphology (morphologic abnormality)
myeloid sarcomas
myelosarcoma
sarcoma granulocytic
sarcoma, granulocytic
sarcoma, granulocytic, malignant
sarcoma, myeloid
sarcoma, myeloid [disease/finding]
sarcoma, myeloid, malignant
sarcomas, granulocytic
sarcomas, myeloid
Orphanet
DOID
UMLS
C0152276
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:31)
C0023418  |  leukemia  |  18
C0023470  |  myeloid leukemia  |  14
C0023467  |  acute myeloid leukemia  |  14
C0023470  |  myelogenous leukemia  |  4
C0023487  |  promyelocytic leukemia  |  3
C0023473  |  chronic myelogenous leukemia  |  3
C0023487  |  acute promyelocytic leukemia  |  3
C0023470  |  myelocytic leukemia  |  3
C0026986  |  myelodysplastic syndrome  |  2
C0023418  |  leukaemia  |  2
C0023470  |  myelogenous leukaemia  |  2
C0008625  |  chromosomal abnormality  |  2
C0012739  |  disseminated intravascular coagulation  |  1
C0836924  |  thrombocythemia  |  1
C0023467  |  acute myeloblastic leukemia  |  1
C0024299  |  malignant lymphoma  |  1
C0015625  |  fanconi anemia  |  1
C0023467  |  acute myelogenous leukaemia  |  1
C0080032  |  malignant pleural effusion  |  1
C0027022  |  myeloid malignancy  |  1
C0040028  |  essential thrombocythemia  |  1
C1261473  |  sarcomas  |  1
C0178879  |  urinary obstruction  |  1
C0700251  |  brachial plexopathy  |  1
C0027022  |  myeloproliferative neoplasms  |  1
C0085669  |  acute leukemia  |  1
C1335437  |  plexopathy  |  1
C0021843  |  intestinal obstruction  |  1
C0023473  |  chronic myeloid leukemia  |  1
C0024299  |  lymphoma  |  1
C0023467  |  acute myelogenous leukemia  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:43)
25  |  ABL1  |  1.621  |  DISEASES
238  |  ALK  |  1.681  |  DISEASES
196527  |  ANO6  |  1.203  |  DISEASES
9332  |  CD163  |  2.775  |  DISEASES
930  |  CD19  |  1.929  |  DISEASES
914  |  CD2  |  1.961  |  DISEASES
962  |  CD48  |  1.13  |  DISEASES
921  |  CD5  |  1.897  |  DISEASES
4267  |  CD99  |  3.045  |  DISEASES
170482  |  CLEC4C  |  1.189  |  DISEASES
8418  |  CMAHP  |  2.567  |  DISEASES
1791  |  DNTT  |  3.159  |  DISEASES
284361  |  EMC10  |  2.901  |  DISEASES
2209  |  FCGR1A  |  1.273  |  DISEASES
81608  |  FIP1L1  |  2.686  |  DISEASES
2526  |  FUT4  |  3.93  |  DISEASES
2811  |  GP1BA  |  1.501  |  DISEASES
2993  |  GYPA  |  2.565  |  DISEASES
3239  |  HOXD13  |  1.175  |  DISEASES
3563  |  IL3RA  |  2.713  |  DISEASES
3683  |  ITGAL  |  1.179  |  DISEASES
3717  |  JAK2  |  1.968  |  DISEASES
3767  |  KCNJ11  |  2.211  |  DISEASES
27040  |  LAT  |  2.718  |  DISEASES
4300  |  MLLT3  |  1.211  |  DISEASES
4311  |  MME  |  1.461  |  DISEASES
4629  |  MYH11  |  3.17  |  DISEASES
5079  |  PAX5  |  1.231  |  DISEASES
55193  |  PBRM1  |  1.318  |  DISEASES
5236  |  PGM1  |  3.671  |  DISEASES
8301  |  PICALM  |  1.124  |  DISEASES
11040  |  PIM2  |  1.331  |  DISEASES
5420  |  PODXL  |  1.001  |  DISEASES
5788  |  PTPRC  |  4.322  |  DISEASES
6239  |  RREB1  |  1.719  |  DISEASES
862  |  RUNX1T1  |  3.368  |  DISEASES
6280  |  S100A9  |  2.727  |  DISEASES
23583  |  SMUG1  |  2.696  |  DISEASES
6693  |  SPN  |  5.397  |  DISEASES
54790  |  TET2  |  3.221  |  DISEASES
9218  |  VAPA  |  2.006  |  DISEASES
7490  |  WT1  |  1.649  |  DISEASES
7750  |  ZMYM2  |  1.548  |  DISEASES
Locus(Waiting for update.)
Disease ID 1312
Disease myeloid sarcoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:18)
Disease ID 1312
Disease myeloid sarcoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:2)
C0700594  |  radiculopathy
C0221383  |  phlegmonous gastritis
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs386626619220413743717JAK2umls:C0152276BeFreeThis report describes the first case of myeloid sarcoma with JAK2 V617F mutation and implication of its progression to AML.0.0005428842011NANANANANA
rs386626619241183743717JAK2umls:C0152276BeFreeIn addition, homozygous JAK2 V617F mutation was detected from the myeloid sarcoma specimen.0.0005428842013NANANANANA
rs77375493241183743717JAK2umls:C0152276BeFreeIn addition, homozygous JAK2 V617F mutation was detected from the myeloid sarcoma specimen.0.0005428842013JAK2;INSL695073770GA,T
rs77375493220413743717JAK2umls:C0152276BeFreeThis report describes the first case of myeloid sarcoma with JAK2 V617F mutation and implication of its progression to AML.0.0005428842011JAK2;INSL695073770GA,T
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 1312
Disease myeloid sarcoma
Case(Waiting for update.)