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Details
Link-It Detail - Human Phenotype - Abnormality of the common coagulation pathway
Debug Stats
  • ### Total Build Time: 21 ms 19.186 KB
  • CONCEPT_NAME gt=4 ms Completed: 3 ms rowSize= 220 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 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=3 ms Completed: 3 ms rowSize= 459 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.736 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 13.273 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.039 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the common coagulation pathway HP:0010990
Definition (1)
An abnormality of `blood coagulation, common pathway` (GO:0072377).
Parents (1)
img Abnormality of the coagulation cascade HP:0003256
Children (5)
img Elevated factor V activity HP:0011996
img Reduced factor X activity HP:0008321
img Reduced factor V activity HP:0003225
img Reduced factor XIII activity HP:0008357
img Abnormality of circulating fibrinogen HP:0011898
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the coagulation cascade HP:0003256
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the coagulation cascade HP:0003256
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanANO6196527anoctamin 6
img HP RolledUp, OMIM ID: 262890
HumanMCFD290411multiple coagulation factor deficiency 2
img HP RolledUp, OMIM ID: 613625
img HP RolledUp, OMIM ID: 227300
HumanVKORC179001vitamin K epoxide reductase complex, subunit 1
img HP RolledUp, OMIM ID: 607473
HumanHPLH127259hemophagocytic lymphohistiocytosis 1
img HP RolledUp, OMIM ID: 267700
HumanSTX118676syntaxin 11
img HP RolledUp, OMIM ID: 603552
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
img HP RolledUp, OMIM ID: 163950
HumanPRF15551perforin 1 (pore forming protein)
img HP RolledUp, OMIM ID: 603553
HumanLMAN13998lectin, mannose-binding, 1
img HP RolledUp, OMIM ID: 227300
HumanGGCX2677gamma-glutamyl carboxylase
img HP RolledUp, OMIM ID: 610842
HumanFGB2244fibrinogen beta chain
img HP RolledUp, OMIM ID: 202400
HumanFGA2243fibrinogen alpha chain
img HP RolledUp, OMIM ID: 202400
HumanF13A12162coagulation factor XIII, A1 polypeptide
img HP RolledUp, OMIM ID: 613225
HumanF102159coagulation factor X
img HP RolledUp, OMIM ID: 227600
HumanF52153coagulation factor V (proaccelerin, labile factor)
img HP RolledUp, OMIM ID: 227400
HumanXIAP331X-linked inhibitor of apoptosis
img HP RolledUp, OMIM ID: 300635
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010990Abnormality of the common coagulation pathway0self