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Details
Link-It Detail - Human Phenotype - Abnormality of circulating fibrinogen
Debug Stats
  • ### Total Build Time: 18 ms 11.139 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 220 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=2 ms Completed: 2 ms rowSize= 466 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.059 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.127 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 5.900 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of circulating fibrinogen HP:0011898
Definition (1)
An abnormality of the level of activity of circulating fibrinogen.
Parents (1)
img Abnormality of the common coagulation pathway HP:0010990
Children (3)
img Dysfibrinogenemia HP:0011901
img Hypofibrinogenemia HP:0011900
img Hyperfibrinogenemia HP:0011899
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the common coagulation pathway HP:0010990
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the common coagulation pathway HP:0010990
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanHPLH127259hemophagocytic lymphohistiocytosis 1
img HP RolledUp, OMIM ID: 267700
HumanSTX118676syntaxin 11
img HP RolledUp, OMIM ID: 603552
HumanPRF15551perforin 1 (pore forming protein)
img HP RolledUp, OMIM ID: 603553
HumanFGB2244fibrinogen beta chain
img HP RolledUp, OMIM ID: 202400
HumanFGA2243fibrinogen alpha chain
img HP RolledUp, OMIM ID: 202400
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:0011898Abnormality of circulating fibrinogen0self