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Details
Link-It Detail - Human Phenotype - Abnormal bleeding
Debug Stats
  • ### Total Build Time: 29 ms 28.562 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 192 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 319 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= 797 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 4.358 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.110 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 19.659 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.012 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal bleeding HP:0001892
Definition (1)
An abnormal susceptibility to bleeding, often referred to as a bleeding diathesis. A bleeding diathesis may be related to vascular, platelet and coagulation defects.
Parents (2)
img Abnormality of blood and blood-forming tissues HP:0001871
img Abnormality of coagulation HP:0001928
Children (13)
img Subcutaneous hemorrhage HP:0001933
img moderate-severe bleeding tendencies HP:0004862
img Internal hemorrhage HP:0011029
img Abnormal umbilical stump bleeding HP:0011884
img Congenital bleeding diathesis HP:0004834
img mild-to-moderate bleeding tendencies HP:0004849
img neonatal bleeding tendency HP:0004830
img Variable bleeding tendencies HP:0008183
img Prolonged bleeding following procedure HP:0011890
img Bleeding requiring red cell transfusion HP:0011888
img Bleeding with minor or no trauma HP:0011889
img moderate bleeding diathesis HP:0004865
img Persistent bleeding after trauma HP:0001934
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of blood and blood-forming tissues HP:0001871
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of coagulation HP:0001928
Genes (237)

Species:
human : 237
Page Size
Current 25
  Page 1 of 10
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
HumanIBD11100529151Inflammatory bowel disease 11
HumanOCLN100506658occludin
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanCISD2493856CDGSH iron sulfur domain 2
img HP PCS, OMIM ID: 604928
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP IEA, OMIM ID: 203300
img HP RolledUp, OMIM ID: 614077
HumanCMAL246230Capillary malformations, hereditary
HumanANO6196527anoctamin 6
img HP TAS, OMIM ID: 262890
HumanTCPT140892thrombocytopenia, Paris-Trousseau type
img HP IEA, OMIM ID: 188025
HumanANIB1116833aneurysm, intracranial berry 1
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
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
HumanMCFD290411multiple coagulation factor deficiency 2
img HP RolledUp, OMIM ID: 613625
img HP IEA, OMIM ID: 227300
HumanHPS489781Hermansky-Pudlak syndrome 4
img HP IEA, OMIM ID: 203300
HumanMASTL84930microtubule associated serine/threonine kinase-like
HumanLCS184565lymphedema-cholestasis syndrome 1
HumanHPS384343Hermansky-Pudlak syndrome 3
img HP TAS, OMIM ID: 614072
img HP IEA, OMIM ID: 203300
HumanDTNBP184062dystrobrevin binding protein 1
img HP IEA, OMIM ID: 203300
img HP RolledUp, OMIM ID: 614076
HumanFERMT383706fermitin family member 3
img HP IEA, OMIM ID: 612840
HumanDOCK881704dedicator of cytokinesis 8
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001892Abnormal bleeding0self