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Details
Link-It Detail - Human Phenotype - Abnormality of the odontoid process
Debug Stats
  • ### Total Build Time: 22 ms 21.749 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 257 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=4 ms Completed: 4 ms rowSize= 456 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.093 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.107 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 16.474 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the odontoid process HP:0003310
Definition (1)
The dens of the axis is a protuberance of the C2 vetebral body around which the first vertebra rotates.
Parents (1)
img Abnormality of the vertebral column HP:0000925
Children (3)
img Abnormal odontoid peg HP:0004600
img Anteriorly placed odontoid process HP:0004608
img Hypoplasia of the odontoid process HP:0003311
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 (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
img HP IEA, OMIM ID: 277300
HumanHES784667hairy and enhancer of split 7 (Drosophila)
img HP IEA, OMIM ID: 613686
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
img HP RolledUp, OMIM ID: 252500
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 184252
HumanDYM54808dymeclin
img HP RolledUp, OMIM ID: 223800
img HP RolledUp, OMIM ID: 607326
HumanDLL310683delta-like 3 (Drosophila)
img HP IEA, OMIM ID: 277300
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img HP RolledUp, OMIM ID: 226980
HumanDDR24921discoidin domain receptor tyrosine kinase 2
img HP RolledUp, OMIM ID: 271665
HumanNFIX4784nuclear factor I/X (CCAAT-binding transcription factor)
img HP RolledUp, OMIM ID: 602535
HumanIDUA3425iduronidase, alpha-L-
img HP RolledUp, OMIM ID: 607014
HumanGUSB2990glucuronidase, beta
img HP RolledUp, OMIM ID: 253220
HumanGLB12720galactosidase, beta 1
img HP RolledUp, OMIM ID: 253010
HumanGALNS2588galactosamine (N-acetyl)-6-sulfate sulfatase
img HP RolledUp, OMIM ID: 253000
HumanFLNB2317filamin B, beta
img HP RolledUp, OMIM ID: 272460
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 305620
HumanFGD12245FYVE, RhoGEF and PH domain containing 1
img HP RolledUp, OMIM ID: 305400
HumanCOMP1311cartilage oligomeric matrix protein
img HP RolledUp, OMIM ID: 177170
HumanCOL2A11280collagen, type II, alpha 1
img HP RolledUp, OMIM ID: 184250
img HP RolledUp, OMIM ID: 183900
img HP RolledUp, OMIM ID: 184252
HumanARSB411arylsulfatase B
img HP RolledUp, OMIM ID: 253200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003310Abnormality of the odontoid process0self