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Details
Link-It Detail - Human Phenotype - Abnormality of the carotid arteries
Debug Stats
  • ### Total Build Time: 17 ms 15.330 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 792 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.062 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.035 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 7.080 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the carotid arteries HP:0005344
Parents (2)
img Systemic artery abnormality HP:0002620
img Abnormality of the systemic arterial tree HP:0011004
Children (9)
img Extracranial internal carotid artery dissection HP:0004945
img Carotid stenosis HP:0100546
img Increased carotid artery intimal medial thickness HP:0012273
img Carotid artery aneurysm HP:0012163
img Carotid artery dissection HP:0012158
img Internal carotid artery hypoplasia HP:0005290
img Carotid artery tortuosity HP:0005302
img Carotid paraganglioma HP:0100635
img Anomalous branches of internal carotid artery HP:0005314
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Systemic artery abnormality HP:0002620
img All HP:0000001img Phenotypic abnormality HP:00001186img Systemic artery abnormality HP:0002620
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the systemic arterial tree HP:0011004
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP TAS, OMIM ID: 208050
HumanMLXIPL51085MLX interacting protein-like
img HP TAS, OMIM ID: 194050
HumanGTF2IRD19569GTF2I repeat domain containing 1
img HP TAS, OMIM ID: 194050
HumanPPARG5468peroxisome proliferator-activated receptor gamma
img HP RolledUp, OMIM ID: 609338
HumanGTF2I2969general transcription factor IIi
img HP TAS, OMIM ID: 194050
HumanELN2006elastin
img HP TAS, OMIM ID: 194050
HumanATP7A538ATPase, Cu++ transporting, alpha polypeptide
img HP TAS, OMIM ID: 309400
img HP RolledUp, OMIM ID: 304150
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005344Abnormality of the carotid arteries0self