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PedAM

Pediatric Disease Annotations & Medicines



   plasmacytoma
  

Disease ID 372
Disease plasmacytoma
Definition
Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites.
Synonym
[m]plasma cell tumor nos
[m]plasma cell tumor nos (morphologic abnormality)
[m]plasma cell tumors
[m]plasma cell tumors (morphologic abnormality)
[m]plasma cell tumour nos
[m]plasma cell tumours
[m]plasmacytoma nos
[m]plasmacytoma nos (disorder)
bone plasmacytoma
monostotic myeloma
myeloma - solitary
myeloma, solitary
plasma cell tumor
plasma cell tumor (clinical)
plasma cell tumor (morphologic abnormality)
plasma cell tumors
plasma cell tumour
plasma cell tumour (clinical)
plasmacytoma (disorder)
plasmacytoma (morphologic abnormality)
plasmacytoma - disorder
plasmacytoma [disease/finding]
plasmacytoma nos (disorder)
plasmacytoma of bone
plasmacytoma, nos
plasmacytomas
plasmacytomas solitary
plasmocytoma
plasmocytomas
solitary myeloma
solitary myeloma (clinical)
solitary plasmacytoma
solitary plasmacytoma of bone
solitary plasmacytoma of bone (morphologic abnormality)
tumor, plasma cell
tumors, plasma cell
Orphanet
DOID
UMLS
C0032131
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:25)
C0026764  |  multiple myeloma  |  24
C0026764  |  myeloma  |  18
C0085404  |  poems syndrome  |  5
C0152025  |  polyneuropathy  |  2
C0007787  |  transient ischemic attacks  |  1
C0029132  |  optic neuropathy  |  1
C0024299  |  lymphoma  |  1
C0019618  |  histiocytosis  |  1
C0001418  |  adenocarcinoma  |  1
C0002726  |  amyloidosis  |  1
C0442874  |  neuropathy  |  1
C0032131  |  solitary myeloma  |  1
C0085110  |  severe combined immunodefic  |  1
C0007102  |  colon cancer  |  1
C0007787  |  transient ischemic attack  |  1
C0010930  |  dacryocystitis  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0152013  |  lung adenocarcinoma  |  1
C0011603  |  dermatitis  |  1
C0011633  |  dermatomyositis  |  1
C0022354  |  obstructive jaundice  |  1
C0019829  |  hodgkin disease  |  1
C0001173  |  gastric outlet obstruction  |  1
C0035078  |  renal failure  |  1
C0017601  |  glaucoma  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:161)
928  |  CD9  |  DISEASES
933  |  CD22  |  DISEASES
5008  |  OSM  |  DISEASES
57617  |  VPS18  |  DISEASES
23581  |  CASP14  |  DISEASES
973  |  CD79A  |  DISEASES
952  |  CD38  |  DISEASES
51056  |  LAP3  |  DISEASES
3558  |  IL2  |  DISEASES
53340  |  SPA17  |  DISEASES
595  |  CCND1  |  DISEASES
4254  |  KITLG  |  DISEASES
57379  |  AICDA  |  DISEASES
1432  |  MAPK14  |  DISEASES
3111  |  HLA-DOA  |  DISEASES
3565  |  IL4  |  DISEASES
3567  |  IL5  |  DISEASES
604  |  BCL6  |  DISEASES
22924  |  MAPRE3  |  DISEASES
7035  |  TFPI  |  DISEASES
10297  |  APC2  |  DISEASES
4109  |  MAGEA10  |  DISEASES
30848  |  CTAG2  |  DISEASES
821  |  CANX  |  DISEASES
968  |  CD68  |  DISEASES
79977  |  GRHL2  |  DISEASES
8572  |  PDLIM4  |  DISEASES
6382  |  SDC1  |  DISEASES
3568  |  IL5RA  |  DISEASES
53  |  ACP2  |  DISEASES
4284  |  MIP  |  DISEASES
3569  |  IL6  |  DISEASES
10113  |  PREB  |  DISEASES
3417  |  IDH1  |  DISEASES
4069  |  LYZ  |  DISEASES
9891  |  NUAK1  |  DISEASES
55745  |  AP5M1  |  DISEASES
8120  |  AP3B2  |  DISEASES
9172  |  MYOM2  |  DISEASES
3595  |  IL12RB2  |  DISEASES
1031  |  CDKN2C  |  DISEASES
5264  |  PHYH  |  DISEASES
7143  |  TNR  |  DISEASES
5067  |  CNTN3  |  DISEASES
943  |  TNFRSF8  |  DISEASES
941  |  CD80  |  DISEASES
3589  |  IL11  |  DISEASES
51726  |  DNAJB11  |  DISEASES
2028  |  ENPEP  |  DISEASES
939  |  CD27  |  DISEASES
1213  |  CLTC  |  DISEASES
7157  |  TP53  |  DISEASES
3578  |  IL9  |  DISEASES
7462  |  LAT2  |  DISEASES
85417  |  CCNB3  |  DISEASES
4103  |  MAGEA4  |  DISEASES
5531  |  PPP4C  |  DISEASES
4613  |  MYCN  |  DISEASES
7070  |  THY1  |  DISEASES
7345  |  UCHL1  |  DISEASES
9947  |  MAGEC1  |  DISEASES
9601  |  PDIA4  |  DISEASES
57466  |  SCAF4  |  DISEASES
4061  |  LY6E  |  DISEASES
84988  |  PPP1R16A  |  DISEASES
85451  |  UNK  |  DISEASES
3678  |  ITGA5  |  DISEASES
2215  |  FCGR3B  |  DISEASES
213  |  ALB  |  DISEASES
10085  |  EDIL3  |  DISEASES
55718  |  POLR3E  |  DISEASES
2923  |  PDIA3  |  DISEASES
147945  |  NLRP4  |  DISEASES
90990  |  KIFC2  |  DISEASES
598  |  BCL2L1  |  DISEASES
10296  |  MAEA  |  DISEASES
1602  |  DACH1  |  DISEASES
7275  |  TUB  |  DISEASES
8028  |  MLLT10  |  DISEASES
25992  |  SNED1  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
80227  |  PAAF1  |  DISEASES
493829  |  TRIM72  |  DISEASES
4684  |  NCAM1  |  DISEASES
6181  |  RPLP2  |  DISEASES
1555  |  CYP2B6  |  DISEASES
4094  |  MAF  |  DISEASES
6938  |  TCF12  |  DISEASES
266740  |  MAGEA2B  |  DISEASES
84186  |  ZCCHC7  |  DISEASES
23583  |  SMUG1  |  DISEASES
2261  |  FGFR3  |  DISEASES
921  |  CD5  |  DISEASES
3005  |  H1F0  |  DISEASES
6189  |  RPS3A  |  DISEASES
2335  |  FN1  |  DISEASES
9260  |  PDLIM7  |  DISEASES
4100  |  MAGEA1  |  DISEASES
3683  |  ITGAL  |  DISEASES
4111  |  MAGEA12  |  DISEASES
5079  |  PAX5  |  DISEASES
841  |  CASP8  |  DISEASES
8021  |  NUP214  |  DISEASES
6693  |  SPN  |  DISEASES
4311  |  MME  |  DISEASES
51660  |  MPC1  |  DISEASES
5167  |  ENPP1  |  DISEASES
1122  |  CHML  |  DISEASES
1380  |  CR2  |  DISEASES
26254  |  OPTC  |  DISEASES
5788  |  PTPRC  |  DISEASES
2329  |  FMO4  |  DISEASES
55827  |  DCAF6  |  DISEASES
3570  |  IL6R  |  DISEASES
4170  |  MCL1  |  DISEASES
639  |  PRDM1  |  DISEASES
4354  |  MPP1  |  DISEASES
4101  |  MAGEA2  |  DISEASES
11146  |  GLMN  |  DISEASES
959  |  CD40LG  |  DISEASES
8880  |  FUBP1  |  DISEASES
7422  |  VEGFA  |  DISEASES
958  |  CD40  |  DISEASES
25  |  ABL1  |  DISEASES
3561  |  IL2RG  |  DISEASES
6668  |  SP2  |  DISEASES
5987  |  TRIM27  |  DISEASES
8928  |  FOXH1  |  DISEASES
4609  |  MYC  |  DISEASES
3559  |  IL2RA  |  DISEASES
3456  |  IFNB1  |  DISEASES
3662  |  IRF4  |  DISEASES
10274  |  STAG1  |  DISEASES
4099  |  MAG  |  DISEASES
974  |  CD79B  |  DISEASES
5450  |  POU2AF1  |  DISEASES
2875  |  GPT  |  DISEASES
1763  |  DNA2  |  DISEASES
8131  |  NPRL3  |  DISEASES
50626  |  CYHR1  |  DISEASES
5965  |  RECQL  |  DISEASES
1719  |  DHFR  |  DISEASES
7124  |  TNF  |  DISEASES
5795  |  PTPRJ  |  DISEASES
84671  |  ZNF347  |  DISEASES
3831  |  KLC1  |  DISEASES
26137  |  ZBTB20  |  DISEASES
80012  |  PHC3  |  DISEASES
4345  |  CD200  |  DISEASES
5238  |  PGM3  |  DISEASES
149466  |  C1orf210  |  DISEASES
100423062  |  IGLL5  |  DISEASES
6188  |  RPS3  |  DISEASES
930  |  CD19  |  DISEASES
5125  |  PCSK5  |  DISEASES
567  |  B2M  |  DISEASES
1506  |  CTRL  |  DISEASES
85316  |  BAGE5  |  DISEASES
103164619  |  PCAT2  |  DISEASES
5820  |  PVT1  |  DISEASES
Locus(Waiting for update.)
Disease ID 372
Disease plasmacytoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:25)
HP:0006775  |  Multiple myeloma  |  24
HP:0001271  |  Polyneuropathy  |  2
HP:0000405  |  Conductive hearing loss  |  1
HP:0002953  |  Vertebral compression fractures  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0002665  |  Lymphoma  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0005202  |  Helicobacter pylori infection  |  1
HP:0030731  |  Carcinoma  |  1
HP:0002326  |  TIA  |  1
HP:0030078  |  Lung adenocarcinoma  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0000620  |  Dacrocystitis  |  1
HP:0003003  |  Colon cancer  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0002664  |  Neoplasia  |  1
HP:0000501  |  Glaucoma  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0002176  |  Spinal cord compression  |  1
HP:0000952  |  Yellow skin  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0002756  |  Pathologic fracture  |  1
Disease ID 372
Disease plasmacytoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:22)
C2364133  |  infection
C1963154  |  renal failure
C1565489  |  renal insufficiency
C1409177  |  paramyloidosis
C1373218  |  immunosuppression
C1000483  |  anemia
C0878544  |  cardiomyopathy
C0850497  |  immune deficiency
C0752303  |  urological manifestations
C0563307  |  igd myeloma
C0432487  |  post-transplant lymphoproliferative disorder
C0400979  |  biliary tract obstruction
C0281479  |  systemic amyloidosis
C0268381  |  al amyloidosis
C0152025  |  polyneuropathy
C0030489  |  paraproteinemia
C0026764  |  myeloma
C0025202  |  malignant melanomas
C0023795  |  hyalinosis cutis et mucosae
C0021051  |  immunodeficiency
C0007137  |  squamous cell carcinoma
C0002726  |  amyloidosis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0026764  |  myeloma  |  17
C0152025  |  polyneuropathy  |  2
C0002726  |  amyloidosis  |  1
C0035078  |  renal failure  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs11348802226071465673BRAFumls:C0032131BeFreeWe analyzed 121 cases, including 26 HCLs, 52 non-HCL splenic lymphomas, 22 chronic lymphocytic leukemias/small lymphocytic lymphomas (CLLs/SLLs), and 21 plasma cell neoplasms (PCNs) for BRAF V600E expression by IHC.0.0002714422015BRAF7140753336AT,G,C
rs2720709173957435820PVT1umls:C0032131BeFreeThese SNPs were genotyped in individuals comprising each pool, and strong evidence for association was found with rs2720709 (P = 0.000021; odds ratio 2.57 [95% CI 1.66-3.96]), which is located in the plasmacytoma variant translocation gene PVT1.0.0010857672007PVT18128046110GA
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.)
Chemical(Total Drugs:3)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0032131bortezomibD000069286-plasmacytomaMESH:D010954therapeutic19259673
C0032131rosiglitazoneC089730-plasmacytomaMESH:D010954therapeutic19731824
C0032131tretinoinD014212302-79-4plasmacytomaMESH:D010954therapeutic19731824
FDA approved drug and dosage information(Total Drugs:1)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D010954velcadebortezomib3.5MG/VIALINJECTABLE;INTRAVENOUS, SUBCUTANEOUSPrescriptionNoneYesYes
FDA labeling changes(Total Drugs:1)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D01095409/14/2015velcadebortezomibRelapsed Acute Lymphoblastic Leukemia (ALL) and Lymphoblastic Lymphoma (LL)Effectiveness in pediatric patients with relapsed pre-B ALL has not been established. The activity and safety of Velcade in combination with intensive reinduction chemotherapy was evaluated in pediatric and young adult patients with lymphoid malignancies. There were 140 patients with ALL or LL enrolled and evaluated for safety. No new safety concerns were observedLabelingB---Millennium Pharmaceuticals, Inc.-FALSE