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Details
Link-It Detail - Disease - Hypoalbuminemia
Debug Stats
  • ### Total Build Time: 94 ms 25.473 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 416 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=0 Completed: 0 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 551 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=19 ms Completed: 19 ms rowSize= 1.511 KB
  • CONCEPT_RELATIONSHIPS gt=22 ms Completed: 22 ms rowSize= 8.140 KB
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 13.193 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypoalbuminemia C0239981
Definition (1)
A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthesis, increased albumin catabolism, altered albumin distribution, or albumin loss through the urine (ALBUMINURIA).
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Hypoproteinemia C0020639
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Hypoproteinemia C0020639
Relationships (19)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 5
diso_​to_​diso : 10
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 18
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM47img Serum Albumin C0036773
DISO_to_ANAT44img In Blood C0005768
DISO_to_DISO40img Complication Aspects C1171258
DISO_to_ANAT26img In Blood C0005768
DISO_to_CHEM23img Serum Albumin C0036773
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_PHEN12img genetic aspects C0017399
DISO_to_CHEM10img Albumins C0001924
DISO_to_DISO10img Kidney Failure, Chronic C0022661
DISO_to_DISO9img Anemia C0002871
DISO_to_DISO9img COMPL POSTOP C0032787
DISO_to_CHEM8img Albumins C0001924
DISO_to_DISO8img Heart Failure C0018801
DISO_to_PHYS6img Blood Pressure C0005823
DISO_to_CHEM5img C-Reactive Protein C0006560
DISO_to_DISO5img Edema C0013604
DISO_to_DISO5img INFECT POSTOP WOUND C0038941
DISO_to_DISO5img Liver Cirrhosis C0023890
DISO_to_DISOmapped_toimg ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA C1859598
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanAPTX54840aprataxin
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanPLCE151196phospholipase C, epsilon 1
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanSAR1B51128SAR1 homolog B (S. cerevisiae)
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
img GENERIF, Score=1000, Pubmed Id: 15690190, UMLKSK CUI: C0239981
HumanSUCLA28803succinate-CoA ligase, ADP-forming, beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanTK27084thymidine kinase 2, mitochondrial
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanPTEN5728phosphatase and tensin homolog
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanPMM25373phosphomannomutase 2
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanMPV174358MpV17 mitochondrial inner membrane protein
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanMPI4351mannose phosphate isomerase
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanSMAD44089SMAD family member 4
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanDGUOK1716deoxyguanosine kinase
img OMIM, Score=1000, UMLKSK CUI: C0239981
HumanBMPR1A657bone morphogenetic protein receptor, type IA
img OMIM, Score=1000, UMLKSK CUI: C0239981
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0239981Hypoalbuminemia0self