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Details
Link-It Detail - Disease - Paraproteinemias
Debug Stats
  • ### Total Build Time: 56 ms 39.211 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 400 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1,006 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.709 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.812 KB
  • CONCEPT_RELATIONSHIPS gt=14 ms Completed: 14 ms rowSize= 12.457 KB
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 18.178 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Paraproteinemias C0030489
Definition (1)
A plasma cell disorder in which an abnormal amount of a single immunoglobulin is present in the serum. Paraproteinemias may be seen in conjunction with various carcinomas, chronic inflammatory and infectious conditions, and other diseases. --2004
Semantic Types (1)
Neoplastic Process (T191)
Parents (2)
img Immunoproliferative Disorders C0021070
img Blood Protein Disorders C0005830
Children (6)
img Monoclonal Gammopathy of Undetermined Significance C0026470
img POEMS Syndrome C0085404
img Heavy Chain Disease C0018852
img Cryoglobulinemia C0010403
img Waldenstrom Macroglobulinemia C0024419
img Multiple Myeloma C0026764
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C0021053img Immunoproliferative Disorders C00210703img Immunoproliferative Disorders C0021070
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Blood Protein Disorders C0005830
Relationships (41)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 17
diso_​to_​diso : 17
diso_​to_​phen : 2


Relationships:
none : 38
isa : 1
permuted_​term_​of : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO171img Complication Aspects C1171258
DISO_to_DISO158img Complication Aspects C1171258
DISO_to_ANAT91img In Blood C0005768
DISO_to_DISO86img Multiple Myeloma C0026764
DISO_to_ANAT61img In Blood C0005768
DISO_to_DISO55img Multiple Myeloma C0026764
DISO_to_CHEM53img Chains, Immunoglobulin Light C0021038
DISO_to_CHEM53img Immunoglobulin Light Chains C0021038
DISO_to_PHEN40img genetic aspects C0017399
DISO_to_PHEN36img genetic aspects C0017399
DISO_to_CHEM31img Immunoglobulin M C0020861
DISO_to_CHEM29img Immunoglobulin kappa-Chains C0021036
DISO_to_CHEM27img Immunoglobulin M C0020861
DISO_to_DISO26img Kidney Diseases C0022658
DISO_to_CHEM25img Chains, Immunoglobulin Light C0021038
DISO_to_DISO25img Amyloidosis C0002726
DISO_to_CHEM24img Immunoglobulin G C0020852
DISO_to_DISO22img Amyloidosis C0002726
DISO_to_DISO22img Peripheral Nervous System Diseases C0031117
DISO_to_CHEM19img Chains, lambda-Immunoglobulin Light C0021037
DISO_to_ANAT18img Plasma Cells C0032112
DISO_to_ANAT16img Plasma Cells C0032112
DISO_to_DISO16img Polyneuropathies C0152025
DISO_to_CHEM15img Immunoglobulin A C0020835
DISO_to_DISO14img Kidney Diseases C0022658
Genes (478)

Species:
human : 478
Page Size
Current 25
  Page 1 of 20
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanSPANXB1728695SPANX family, member B1
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanCSAG2728461CSAG family, member 2
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanGGT2728441gamma-glutamyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanPPBPL1728045
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanIL29282618
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanST13P4145165suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 4
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanMIB2142678mindbomb E3 ubiquitin protein ligase 2
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanHIST3H2BB128312histone cluster 3, H2bb
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanSP7121340Sp7 transcription factor
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanMUC1694025mucin 16, cell surface associated
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanTUBA1C84790tubulin, alpha 1c
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanINHBE83729inhibin, beta E
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanFCRL483417Fc receptor-like 4
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanFCRL583416Fc receptor-like 5
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanCOL18A180781collagen, type XVIII, alpha 1
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanMLVI466001Moloney leukemia virus integration site 4, mouse, homolog of
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanTPSB264499tryptase beta 2 (gene/pseudogene)
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanSAMSN164092SAM domain, SH3 domain and nuclear localization signals 1
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanIL2159067interleukin 21
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanSLAMF757823SLAM family member 7
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanAICDA57379activation-induced cytidine deaminase
INFERRED, Score=800, UMLKSK CUI: C0030489
HumanC8orf1756988chromosome 8 open reading frame 17
INFERRED, Score=800, UMLKSK CUI: C0030489
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030489Paraproteinemias0self