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Details
Link-It Detail - Human Phenotype - Abnormality of the intervertebral disk
Debug Stats
  • ### Total Build Time: 17 ms 11.886 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 213 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 210 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= 456 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.429 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.107 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 6.314 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.032 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the intervertebral disk HP:0005108
Definition (1)
An abnormality of the `intervertebral disk` (FMA:10446).
Parents (1)
img Abnormality of the vertebral column HP:0000925
Children (4)
img Herniation of intervertebral nuclei HP:0008441
img Intervertebral disc degeneration HP:0008419
img Intervertebral disk calcification HP:0005645
img Intervertebral space narrowing HP:0002945
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the vertebral column HP:0000925
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the vertebral column HP:0000925
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP TAS, OMIM ID: 156530
HumanCHST39469carbohydrate (chondroitin 6) sulfotransferase 3
img HP RolledUp, OMIM ID: 608637
img HP RolledUp, OMIM ID: 143095
HumanSHOC28036soc-2 suppressor of clear homolog (C. elegans)
img HP TAS, OMIM ID: 607721
HumanSMAD34088SMAD family member 3
img HP RolledUp, OMIM ID: 613795
HumanHOXD133239homeobox D13
img HP TAS, OMIM ID: 192350
HumanHGD3081homogentisate 1,2-dioxygenase
img HP RolledUp, OMIM ID: 203500
HumanCOL2A11280collagen, type II, alpha 1
img HP RolledUp, OMIM ID: 609162
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005108Abnormality of the intervertebral disk0self