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Details
Link-It Detail - Disease - AVM - Cerebral arteriovenous malformation
Debug Stats
  • ### Total Build Time: 43 ms 5.480 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 442 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 3.329 KB
  • CONCEPT_XREFS gt=14 ms Completed: 14 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
AVM - Cerebral arteriovenous malformation C0917804
Definition (1)
An abnormal connection between arteries and veins characterized by the absence of intervening capillaries in the brain. Signs and symptoms include headaches, bruit upon headl examination, seizures, and bleeding. When bleeding occurs, the signs and symptoms are similar to those in stroke.
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanVEGFA7422vascular endothelial growth factor A
img GENERIF, Score=1000, Pubmed Id: 16388189, UMLKSK CUI: C0917804
HumanENG2022endoglin
img OMIM, Score=1000, UMLKSK CUI: C0917804
HumanACVRL194activin A receptor type II-like 1
img OMIM, Score=1000, UMLKSK CUI: C0917804
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0917804AVM - Cerebral arteriovenous malformation0self