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Details
Link-It Detail - Human Phenotype - Abnormalities of placenta and umbilical cord
Debug Stats
  • ### Total Build Time: 20 ms 27.358 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 219 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= 465 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.353 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.180 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 21.976 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormalities of placenta and umbilical cord HP:0001194
Parents (1)
img Abnormality of prenatal development or birth HP:0001197
Children (7)
img Abnormality of the umbilical cord HP:0010881
img Single umbilical artery HP:0001195
img Short umbilical cord HP:0001196
img Large placenta HP:0006267
img Abnormality of the placenta HP:0100767
img Abnormality of placental membranes HP:0011409
img Small placenta HP:0006266
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of prenatal development or birth HP:0001197
Genes (29)

Species:
human : 29
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDOK7285489docking protein 7
img HP RolledUp, OMIM ID: 208150
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
HumanMRXSA57791Armfield X-linked mental retardation syndrome
img HP RolledUp, OMIM ID: 300261
HumanFERMT155612fermitin family member 1
img HP RolledUp, OMIM ID: 173650
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 249000
HumanPOMP51371proteasome maturation protein
img HP RolledUp, OMIM ID: 601952
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
img HP RolledUp, OMIM ID: 300404
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img HP RolledUp, OMIM ID: 308050
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 275210
HumanTTC379652tetratricopeptide repeat domain 37
img HP IEA, OMIM ID: 222470
HumanWNT37473wingless-type MMTV integration site family, member 3
img HP RolledUp, OMIM ID: 273395
HumanRAPSN5913receptor-associated protein of the synapse
img HP RolledUp, OMIM ID: 208150
HumanPOR5447P450 (cytochrome) oxidoreductase
img HP IEA, OMIM ID: 201750
HumanLOR4014loricrin
img HP RolledUp, OMIM ID: 602036
HumanLMNA4000lamin A/C
img HP RolledUp, OMIM ID: 275210
HumanHOXD133239homeobox D13
img HP RolledUp, OMIM ID: 192350
HumanGLE12733GLE1 RNA export mediator
img HP RolledUp, OMIM ID: 253310
HumanGJB22706gap junction protein, beta 2, 26kDa
img HP RolledUp, OMIM ID: 124500
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:0001194Abnormalities of placenta and umbilical cord0self