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Details
Link-It Detail - Human Phenotype - Abnormal sternal ossification
Debug Stats
  • ### Total Build Time: 1,105 ms 15.284 KB
  • CONCEPT_NAME gt=248 ms Completed: 248 ms rowSize= 204 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 234 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=3 ms Completed: 3 ms rowSize= 776 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.441 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 3.946 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=848 ms Completed: 848 ms rowSize= 7.543 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Human Phenotype (1)
Abnormal sternal ossification HP:0011863
Definition (1)
Any anomaly in the formation of the bony substance of the `sternum` (FMA:7485).
Parents (2)
img Abnormality of the sternum HP:0000766
img Abnormal bone ossification HP:0011849
Children (4)
img Absent sternal ossification HP:0006628
img Fused sternal ossification centers HP:0006643
img Large sternal ossification centers HP:0006642
img Decreased number of sternal ossification centers HP:0006611
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the sternum HP:0000766
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the sternum HP:0000766
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormal bone ossification HP:0011849
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal bone ossification HP:0011849
Genes (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanORC623594origin recognition complex, subunit 6
img HP RolledUp, OMIM ID: 613803
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 211750
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
img HP RolledUp, OMIM ID: 216340
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img HP TAS, OMIM ID: 194190
HumanWHCR7467Wolf-Hirschhorn syndrome chromosome region
img HP TAS, OMIM ID: 194190
HumanSOX96662SRY (sex determining region Y)-box 9
img HP RolledUp, OMIM ID: 114290
HumanORC14998origin recognition complex, subunit 1
img HP RolledUp, OMIM ID: 224690
HumanNFIX4784nuclear factor I/X (CCAAT-binding transcription factor)
img HP RolledUp, OMIM ID: 602535
HumanGJA12697gap junction protein, alpha 1, 43kDa
img HP RolledUp, OMIM ID: 234100
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011863Abnormal sternal ossification0self