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Details
Link-It Detail - Disease - Factor X Deficiency
Debug Stats
  • ### Total Build Time: 19 ms 18.587 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 281 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= 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=6 ms Completed: 6 ms rowSize= 5.443 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 7.521 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 2.221 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Factor X Deficiency C0015519
Definition (1)
A rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor X, resulting in bleeding.
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 (14)

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


Relationships:
none : 8
entry_​version_​of : 1
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
isa : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN25img genetic aspects C0017399
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_CHEM18img Factor X C0015518
DISO_to_ANAT9img In Blood C0005768
DISO_to_DISO9img Amyloidosis C0002726
DISO_to_PHYS9img Mutation C0026882
DISO_to_PHYS8img Missense Mutation C0599155
DISO_to_ANAT7img In Blood C0005768
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 Stuart factor deficiency disease C0272328
DISO_to_DISOentry_version_ofimg Factor X Deficiency C0015519
DISO_to_DISOisaimg Hereditary Stuart factor deficiency disease C0272327
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanF102159coagulation factor X
img GENERIF, Score=923, Pubmed Id: 18245654, UMLKSK CUI: C0015519
img GENERIF, Score=923, Pubmed Id: 18403394, UMLKSK CUI: C0015519
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015519Factor X Deficiency0self