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Details
Link-It Detail - Human Phenotype - Abnormality of dental structure
Debug Stats
  • ### Total Build Time: 27 ms 27.479 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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=0 Completed: 0 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.353 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 21.952 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of dental structure HP:0011061
Definition (1)
An abnormality of the structure or composition of the teeth.
Parents (1)
img Abnormality of the teeth HP:0000164
Children (7)
img Carious teeth HP:0000670
img Abnormality of the dental pulp HP:0006479
img Abnormality of dental color HP:0011073
img Abnormality of dental enamel HP:0000682
img Abnormality of dentin HP:0010299
img Hypoplasia of teeth HP:0000685
img Abnormality of the cementum HP:0100717
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (180)

Species:
human : 180
Page Size
Current 25
  Page 1 of 8
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanKIF7374654kinesin family member 7
img HP RolledUp, OMIM ID: 200990
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanFAM83H286077family with sequence similarity 83, member H
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanWDR72256764WD repeat domain 72
img HP RolledUp, OMIM ID: 613211
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
HumanTRPV3162514transient receptor potential cation channel, subfamily V, member 3
img HP RolledUp, OMIM ID: 614594
HumanC4orf26152816chromosome 4 open reading frame 26
img HP RolledUp, OMIM ID: 614832
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanMPLKIP136647M-phase specific PLK1 interacting protein
img HP RolledUp, OMIM ID: 234050
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanC12orf57113246chromosome 12 open reading frame 57
img HP RolledUp, OMIM ID: 218340
HumanIFT43112752intraflagellar transport 43 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 614099
HumanCOX4I284701cytochrome c oxidase subunit IV isoform 2 (lung)
img HP RolledUp, OMIM ID: 612714
HumanZNF46984627zinc finger protein 469
HumanPVRL481607poliovirus receptor-related 4
img HP RolledUp, OMIM ID: 613573
HumanROGDI79641rogdi homolog (Drosophila)
img HP RolledUp, OMIM ID: 226750
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011061Abnormality of dental structure0self