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Details
Link-It Detail - Disease - Hypofibrinogenemia
Debug Stats
  • ### Total Build Time: 68 ms 13.491 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 261 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=35 ms Completed: 35 ms rowSize= 4.152 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 7.535 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypofibrinogenemia C0553681
Definition (1)
A blood coagulation disorder characterized by low levels of fibrinogen in the blood, resulting in bleeding.
Relationships (6)

Relation Types:
diso_​to_​anat : 3
diso_​to_​diso : 3


Relationships:
associated_​with : 2
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
isa : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_associated_anatomic_site_ofimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_DISOisaimg Acquired hypofibrinogenaemia C0392609
DISO_to_DISOassociated_withimg Antepartum haemorrhage with hypofibrinogenaemia C0473370
DISO_to_DISOassociated_withimg Parturient haemorrhage associated with hypofibrinogenaemia C0269616
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanFGG2266fibrinogen gamma chain
img GENERIF, Score=827, Pubmed Id: 18000621, UMLKSK CUI: C0553681
img GENERIF, Score=1000, Pubmed Id: 17849064, UMLKSK CUI: C0553681
img GENERIF, Score=861, Pubmed Id: 17650452, UMLKSK CUI: C0553681
HumanFGB2244fibrinogen beta chain
img GENERIF, Score=1000, Pubmed Id: 17849064, UMLKSK CUI: C0553681
img GENERIF, Score=827, Pubmed Id: 18000621, UMLKSK CUI: C0553681
img GENERIF, Score=1000, Pubmed Id: 16601848, UMLKSK CUI: C0553681
img GENERIF, Score=795, Pubmed Id: 16953282, UMLKSK CUI: C0553681
HumanFGA2243fibrinogen alpha chain
img GENERIF, Score=1000, Pubmed Id: 17849064, UMLKSK CUI: C0553681
img GENERIF, Score=1000, Pubmed Id: 16894470, UMLKSK CUI: C0553681
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0553681Hypofibrinogenemia0self