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Details
Link-It Detail - Disease - Hypoproteinemia
Debug Stats
  • ### Total Build Time: 126 ms 25.426 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 336 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 553 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=18 ms Completed: 18 ms rowSize= 1.519 KB
  • CONCEPT_RELATIONSHIPS gt=40 ms Completed: 40 ms rowSize= 6.311 KB
  • CONCEPT_GENES gt=32 ms Completed: 32 ms rowSize= 14.461 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hypoproteinemia C0020639
HYPOPROTEINAEMIA
Definition (1)
A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Blood Protein Disorders C0005830
Children (1)
img Hypoalbuminemia C0239981
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Blood Protein Disorders C0005830
Relationships (14)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 3
diso_​to_​diso : 10


Relationships:
none : 10
mapped_​to : 3
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_ANAT8img In Blood C0005768
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_DISO5img Edema C0013604
DISO_to_DISO4img Respiratory Distress Syndrome, Adult C0035222
DISO_to_CHEM3img Diuretics C0012798
DISO_to_CHEM3img Furosemide C0016860
DISO_to_CHEM3img Serum Albumin C0036773
DISO_to_DISO3img Anemia C0002871
DISO_to_DISO3img Anemia, Iron-Deficiency C0162316
DISO_to_DISOmapped_toimg Albumin serum plasma decreased C0541768
DISO_to_DISOmapped_toimg Decreased serum protein level C0392692
DISO_to_DISOpermuted_term_ofimg HYPOPROTEINAEMIA C0020639
DISO_to_DISOmapped_toimg Hypoalbuminemia C0239981
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanDCLRE1C64421DNA cross-link repair 1C
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanC10orf256652chromosome 10 open reading frame 2
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanAPTX54840aprataxin
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanPLCE151196phospholipase C, epsilon 1
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanSAR1B51128SAR1 homolog B (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanSUCLA28803succinate-CoA ligase, ADP-forming, beta subunit
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanTK27084thymidine kinase 2, mitochondrial
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanRAG25897recombination activating gene 2
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanRAG15896recombination activating gene 1
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanPTEN5728phosphatase and tensin homolog
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanPMM25373phosphomannomutase 2
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanMPV174358MpV17 mitochondrial inner membrane protein
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanMPI4351mannose phosphate isomerase
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanSMAD44089SMAD family member 4
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanLAMB23913laminin, beta 2 (laminin S)
img OMIM, Score=1000, UMLKSK CUI: C0020639
HumanDGUOK1716deoxyguanosine kinase
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanBMPR1A657bone morphogenetic protein receptor, type IA
INFERRED, Score=800, UMLKSK CUI: C0020639
HumanB2M567beta-2-microglobulin
img OMIM, Score=1000, UMLKSK CUI: C0020639
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020639Hypoproteinemia0self