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Details
Link-It Detail - Human Phenotype - Abnormality of the cervical spine
Debug Stats
  • ### Total Build Time: 31 ms 34.823 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 208 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=3 ms Completed: 3 ms rowSize= 456 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 6.618 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=20 ms Completed: 20 ms rowSize= 24.065 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cervical spine HP:0003319
Definition (1)
Any abnormality of the `cervical vertebral column` (FMA:24138).
Parents (1)
img Abnormality of the vertebral column HP:0000925
Children (20)
img Cervical subluxation HP:0003308
img Decreased cervical spine mobility HP:0004637
img Cervical vertebral facet hypoplasia HP:0008461
img Cervical platyspondyly HP:0004558
img C1-C2 vertebral abnormality HP:0008440
img Cervical kyphosis HP:0002947
img Enlarged sagittal diameter of the cervical canal HP:0005878
img Cervical spine hypermobility HP:0003318
img Abnormal cervical curvature HP:0005905
img Cervical spondylosis HP:0008480
img Hypoplastic cervical vertebrae HP:0008434
img Aplasia/Hypoplasia of the cervical spine HP:0011041
img Cervical vertebral dysplasia HP:0008469
img Cervical vertebral agenesis HP:0008459
img Widening of cervical spinal canal HP:0004571
img Short neck HP:0000470
img C2-C3 subluxation HP:0008456
img Cervical spine instability HP:0010646
img Poorly ossified cervical vertebrae HP:0008477
img Cervical vertebral bodies with decreased anteroposterior diameter HP:0008483
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 (184)

Species:
human : 184
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanDUP17P13.3100379203
img HP RolledUp, OMIM ID: 613215
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanGDF6392255growth differentiation factor 6
img HP RolledUp, OMIM ID: 118100
img HP RolledUp, OMIM ID: 122600
img HP RolledUp, OMIM ID: 148900
img HP RolledUp, OMIM ID: 214300
HumanDOK7285489docking protein 7
img HP RolledUp, OMIM ID: 208150
HumanMMEDF260403Macrocephaly with multiple epiphyseal dysplasia and distinctive facies
img HP RolledUp, OMIM ID: 607131
HumanBMPER168667BMP binding endothelial regulator
img HP RolledUp, OMIM ID: 608022
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
img HP RolledUp, OMIM ID: 611431
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003319Abnormality of the cervical spine0self