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Details
Link-It Detail - Disease - Afibrinogenemia
Debug Stats
  • ### Total Build Time: 141 ms 25.461 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= 205 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 1.427 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=34 ms Completed: 34 ms rowSize= 5.443 KB
  • CONCEPT_RELATIONSHIPS gt=66 ms Completed: 66 ms rowSize= 9.885 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 6.817 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Afibrinogenemia C0001733
Definition (1)
A deficiency or absence of FIBRINOGEN in the blood.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Hemorrhagic Disorders C0019087
img Coagulation Protein Disorders C0600503
img Blood Coagulation Disorders, Inherited C0852077
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Hemorrhagic Disorders C0019087
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Coagulation Protein Disorders C0600503
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Blood Coagulation Disorders, Inherited C0852077
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501234img Blood Coagulation Disorders, Inherited C0852077
Relationships (20)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 4
diso_​to_​diso : 10
diso_​to_​phen : 2


Relationships:
none : 9
associated_​with : 2
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 4
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM58img Fibrinogen C0016006
DISO_to_PHEN57img genetic aspects C0017399
DISO_to_PHEN54img genetic aspects C0017399
DISO_to_CHEM48img Fibrinogen C0016006
DISO_to_DISO37img Complication Aspects C1171258
DISO_to_ANAT30img In Blood C0005768
DISO_to_DISO27img Complication Aspects C1171258
DISO_to_CHEM22img ABNORM FIBRINOGENS C0016013
DISO_to_CHEM22img Fibrinogens, Abnormal C0016013
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_DISOisaimg Acquired afibrinogenaemia C1260902
DISO_to_DISOisaimg Afibrinogenaemia - postpartum C0341976
DISO_to_DISOpermuted_term_ofimg Afibrinogenemia C0001733
DISO_to_DISOassociated_withimg Antepartum haemorrhage with afibrinogenaemia C0473372
DISO_to_DISOisaimg Hereditary Factor I Deficiency C3274492
DISO_to_DISOmapped_toimg Hereditary factor I deficiency disease C0019250
DISO_to_DISOisaimg Hypofibrinogenemia C0553681
DISO_to_DISOassociated_withimg Parturient haemorrhage associated with afibrinogenaemia C0269614
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanCFI3426complement factor I
img GENERIF, Score=937, Pubmed Id: 19065647, UMLKSK CUI: C0001733
img GENERIF, Score=1000, Pubmed Id: 18374984, UMLKSK CUI: C0001733
HumanFGG2266fibrinogen gamma chain
img GENERIF, Score=1000, Pubmed Id: 17854317, UMLKSK CUI: C0001733
HumanFGB2244fibrinogen beta chain
img OMIM, Score=1000, UMLKSK CUI: C0001733
HumanFGA2243fibrinogen alpha chain
img GENERIF, Score=1000, Pubmed Id: 17295221, UMLKSK CUI: C0001733
img OMIM, Score=1000, UMLKSK CUI: C0001733
HumanCR11378complement component (3b/4b) receptor 1 (Knops blood group)
img GENERIF, Score=1000, Pubmed Id: 12490287, UMLKSK CUI: C0001733
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0001733Afibrinogenemia0self