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Details
Link-It Detail - Human Phenotype - Abnormality of the parietal bone
Debug Stats
  • ### Total Build Time: 20 ms 21.581 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 217 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=2 ms Completed: 2 ms rowSize= 786 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.076 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.903 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 13.249 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the parietal bone HP:0002696
Definition (1)
Any abnormality of the `parietal bone` (FMA:9613) of the skull.
Parents (2)
img Abnormality of the calvaria HP:0002683
img Abnormality of calvarial morphology HP:0002648
Children (3)
img Symmetrical, oval parietal bone defects HP:0002695
img Parietal foramina HP:0002697
img Parietal bossing HP:0000242
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the calvaria HP:0002683
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the calvaria HP:0002683
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of calvarial morphology HP:0002648
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of calvarial morphology HP:0002648
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of calvarial morphology HP:0002648
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanPSS780904Potocki-Shaffer syndrome
img HP RolledUp, OMIM ID: 601224
HumanPFM3619475parietal foramina 3
img HP RolledUp, OMIM ID: 609566
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
HumanDBA2114086Diamond-Blackfan anemia 2
img HP RolledUp, OMIM ID: 105650
HumanALX460529ALX homeobox 4
img HP RolledUp, OMIM ID: 168500
img HP RolledUp, OMIM ID: 609597
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
img HP RolledUp, OMIM ID: 101400
HumanRPS196223ribosomal protein S19
img HP RolledUp, OMIM ID: 105650
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
img HP RolledUp, OMIM ID: 151100
HumanPTCH15727patched 1
img HP RolledUp, OMIM ID: 610828
img HP RolledUp, OMIM ID: 109400
HumanMSX24488msh homeobox 2
img HP RolledUp, OMIM ID: 168550
img HP RolledUp, OMIM ID: 168500
HumanGJA12697gap junction protein, alpha 1, 43kDa
img HP RolledUp, OMIM ID: 234100
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 101400
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanRUNX2860runt-related transcription factor 2
img HP RolledUp, OMIM ID: 119600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002696Abnormality of the parietal bone0self