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Details
Link-It Detail - Human Phenotype - Abnormality of the fetal cardiovascular system
Debug Stats
  • ### Total Build Time: 8 ms 14.505 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 221 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= 461 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 2.414 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 9.064 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.040 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the fetal cardiovascular system HP:0010948
Parents (1)
img Abnormality of the cardiovascular system HP:0001626
Children (7)
img Abnormality of ductus venosus blood flow HP:0010947
img Echogenic intracardiac focus HP:0010942
img Persistent fetal circulation HP:0011726
img Congenital portosystemic venous shunt HP:0012022
img Single umbilical artery HP:0001195
img Persistent patent ductus venosus HP:0012021
img Abnormality of umbilical vein blood flow HP:0010949
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the cardiovascular system HP:0001626
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanADAMTS18170692ADAM metallopeptidase with thrombospondin type 1 motif, 18
img HP RolledUp, OMIM ID: 608454
HumanSCARF291179scavenger receptor class F, member 2
img HP RolledUp, OMIM ID: 600920
HumanVANGL181839VANGL planar cell polarity protein 1
img HP RolledUp, OMIM ID: 600145
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 249000
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
img HP RolledUp, OMIM ID: 300404
HumanWNT37473wingless-type MMTV integration site family, member 3
img HP RolledUp, OMIM ID: 273395
HumanHOXD133239homeobox D13
img HP RolledUp, OMIM ID: 192350
HumanFOXF12294forkhead box F1
img HP RolledUp, OMIM ID: 265380
HumanCPS11373carbamoyl-phosphate synthase 1, mitochondrial
img HP RolledUp, OMIM ID: 265380
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010948Abnormality of the fetal cardiovascular system0self