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Details
Link-It Detail - Human Phenotype - Abnormality of blood circulation
Debug Stats
  • ### Total Build Time: 227 ms 22.605 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 207 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=0 Completed: 0 ms rowSize= 468 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.085 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.183 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=226 ms Completed: 226 ms rowSize= 18.508 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of blood circulation HP:0011028
Parents (1)
img Abnormality of cardiovascular system physiology HP:0011025
Children (3)
img Abnormality of blood volume homeostasis HP:0011104
img Subcutaneous hemorrhage HP:0001933
img Internal hemorrhage HP:0011029
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of cardiovascular system physiology HP:0011025
Genes (216)

Species:
human : 216
Page Size
Current 25
  Page 1 of 9
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanIBD11100529151Inflammatory bowel disease 11
HumanOCLN100506658occludin
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP RolledUp, OMIM ID: 614077
HumanCMAL246230Capillary malformations, hereditary
img HP RolledUp, OMIM ID: 163000
HumanANIB1116833aneurysm, intracranial berry 1
img HP RolledUp, OMIM ID: 105800
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 120100
img HP RolledUp, OMIM ID: 607115
HumanCHST14113189carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
img HP RolledUp, OMIM ID: 601776
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
HumanHPS489781Hermansky-Pudlak syndrome 4
HumanMASTL84930microtubule associated serine/threonine kinase-like
HumanLCS184565lymphedema-cholestasis syndrome 1
img HP RolledUp, OMIM ID: 214900
HumanHPS384343Hermansky-Pudlak syndrome 3
HumanDTNBP184062dystrobrevin binding protein 1
img HP RolledUp, OMIM ID: 614076
HumanFERMT383706fermitin family member 3
HumanDOCK881704dedicator of cytokinesis 8
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
HumanHSD3B780270hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
img HP RolledUp, OMIM ID: 607765
HumanCTC180169CTS telomere maintenance complex component 1
HumanHPS679803Hermansky-Pudlak syndrome 6
HumanRHBDF279651rhomboid 5 homolog 2 (Drosophila)
img HP RolledUp, OMIM ID: 148500
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011028Abnormality of blood circulation0self