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Details
Link-It Detail - Disease - Factor VII Deficiency
Debug Stats
  • ### Total Build Time: 42 ms 27.240 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 368 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=4 ms Completed: 4 ms rowSize= 1.427 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 5.443 KB
  • CONCEPT_RELATIONSHIPS gt=19 ms Completed: 19 ms rowSize= 13.371 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 4.934 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Factor VII Deficiency C0015503
Definition (1)
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.
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 Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501234img Blood Coagulation Disorders, Inherited C0852077
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Blood Coagulation Disorders, Inherited C0852077
Relationships (39)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 22
diso_​to_​diso : 13
diso_​to_​phen : 2


Relationships:
none : 9
isa : 2
manifestation_​of : 8
may_​treat : 19
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN61img genetic aspects C0017399
DISO_to_CHEM51img Blood Coagulation Factor VII C0015502
DISO_to_PHEN48img genetic aspects C0017399
DISO_to_CHEM39img Blood Coagulation Factor VII C0015502
DISO_to_DISO36img Complication Aspects C1171258
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_ANAT24img In Blood C0005768
DISO_to_ANAT18img In Blood C0005768
DISO_to_CHEM16img Factor VIIa C0015505
DISO_to_CHEMmay_treatimg ANTIHEMOPH.FVIII PLAS/ALB FREE 1,000 (+/-) unit INTRAVEN. VIAL (SDV,MDV OR ADDITIVE) (EA) C2343047
DISO_to_CHEMmay_treatimg ANTIHEMOPH.FVIII PLAS/ALB FREE 2,000 (+/-) unit INTRAVEN. VIAL (SDV,MDV OR ADDITIVE) (EA) C2343044
DISO_to_CHEMmay_treatimg ANTIHEMOPH.FVIII PLAS/ALB FREE 3,000 (+/-) unit INTRAVEN. VIAL (SDV,MDV OR ADDITIVE) (EA) C2356721
DISO_to_CHEMmay_treatimg ANTIHEMOPH.FVIII PLAS/ALB FREE 500 (+/-) unit INTRAVEN. VIAL (SDV,MDV OR ADDITIVE) (EA) C1589768
DISO_to_CHEMmay_treatimg ANTIHEMOPHILIC FACTOR,HUMAN 310 (+/-) unit (220 unit-400 unit) INTRAVEN VIAL (SDV,MDV OR ADDITIVE) (EA) C2343026
DISO_to_CHEMmay_treatimg ANTIHEMOPHILIC FACTOR,HUMAN INJ C0974447
DISO_to_CHEMmay_treatimg ANTIHEMOPHILIC FACTOR,HUMAN,METHOD M,MONOCLONAL C0991795
DISO_to_CHEMmay_treatimg ANTIHEMOPHILIC FACTOR,PORCINE 400UNT/VIL INJ C0974449
DISO_to_CHEMmay_treatimg ANTIHEMOPHILIC FACTOR,RECOMBINANT C1443674
DISO_to_CHEMmay_treatimg Antihemophilic factor, porcine C0724529
DISO_to_CHEMmay_treatimg COAGULATION FACTOR IX RECOMBINANT 250 UNT INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION C1621474
DISO_to_CHEMmay_treatimg Coagulation Factor VIIa (Recomb) For Inj 1200 MCG C2344216
DISO_to_CHEMmay_treatimg Coagulation Factor VIIa (Recomb) For Inj 2400 MCG C0976854
DISO_to_CHEMmay_treatimg FACTOR IX,RECOMBINANT C0982152
DISO_to_CHEMmay_treatimg FACTOR IX,RECOMBINANT 500 UNT/VIL INJ C0976852
DISO_to_CHEMmay_treatimg FACTOR VIIa,RECOMBINANT C0534191
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanF82157coagulation factor VIII, procoagulant component
img GAD, Score=1000, Pubmed Id: 12935978, UMLKSK CUI: C0015503
HumanF72155coagulation factor VII (serum prothrombin conversion accelerator)
img GENERIF, Score=884, Pubmed Id: 18156490, UMLKSK CUI: C0015503
img GAD, Score=1000, Pubmed Id: 15735798, UMLKSK CUI: C0015503
img GENERIF, Score=717, Pubmed Id: 15456489, UMLKSK CUI: C0015503
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015503Factor VII Deficiency0self